ENST00000651892.2:c.-99G>T
(CPLANE1)
MANE Select
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ENSP00000498265.2:n.-99G>T
|
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ENST00000675547.1:n.70G>T
(CPLANE1)
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ENST00000425232.6:c.-99G>T
(CPLANE1)
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ENSP00000389014.2:n.-99G>T
|
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NM_023073.3:c.-99G>T
(CPLANE1)
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NP_075561.3:n.-99G>T
|
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XM_005248345.2:c.-99G>T
(CPLANE1)
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XP_005248402.1:n.-99G>T
|
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XM_005248346.2:c.-99G>T
(CPLANE1)
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XP_005248403.1:n.-99G>T
|
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XM_005248347.2:c.-99G>T
(CPLANE1)
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XP_005248404.1:n.-99G>T
|
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XM_005248349.2:c.-99G>T
(CPLANE1)
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XP_005248406.1:n.-99G>T
|
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XM_005248350.2:c.-99G>T
(CPLANE1)
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XP_005248407.1:n.-99G>T
|
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XM_006714489.2:c.-99G>T
(CPLANE1)
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XP_006714552.1:n.-99G>T
|
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XM_011514086.1:c.-142G>T
(CPLANE1)
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XP_011512388.1:n.-142G>T
|
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XM_011514087.1:c.-99G>T
(CPLANE1)
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XP_011512389.1:n.-99G>T
|
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XM_011514088.1:c.-99G>T
(CPLANE1)
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XP_011512390.1:n.-99G>T
|
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XM_011514089.1:c.-99G>T
(CPLANE1)
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XP_011512391.1:n.-99G>T
|
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XM_011514090.1:c.-336G>T
(CPLANE1)
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XP_011512392.1:n.-336G>T
|
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XM_011514092.1:c.-99G>T
(CPLANE1)
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XP_011512394.1:n.-99G>T
|
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XM_011514093.1:c.-99G>T
(CPLANE1)
|
XP_011512395.1:n.-99G>T
|
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XR_427661.2:n.77G>T
(CPLANE1)
|
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XR_925644.1:n.77G>T
(CPLANE1)
|
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XR_925921.1:n.171+75C>A
(CPLANE1-AS1)
|
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NR_134263.1:n.176+75C>A
(CPLANE1-AS1)
|
|
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XM_005248345.4:c.-99G>T
(CPLANE1)
|
XP_005248402.1:n.-99G>T
|
|
XM_005248346.4:c.-99G>T
(CPLANE1)
|
XP_005248403.1:n.-99G>T
|
|
XM_005248347.4:c.-99G>T
(CPLANE1)
|
XP_005248404.1:n.-99G>T
|
|
XM_005248349.4:c.-99G>T
(CPLANE1)
|
XP_005248406.1:n.-99G>T
|
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XM_005248350.4:c.-99G>T
(CPLANE1)
|
XP_005248407.1:n.-99G>T
|
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XM_011514086.3:c.-142G>T
(CPLANE1)
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XP_011512388.1:n.-142G>T
|
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XM_011514087.2:c.-99G>T
(CPLANE1)
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XP_011512389.1:n.-99G>T
|
|
XM_011514088.2:c.-99G>T
(CPLANE1)
|
XP_011512390.1:n.-99G>T
|
|
XM_011514089.2:c.-99G>T
(CPLANE1)
|
XP_011512391.1:n.-99G>T
|
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XM_011514090.3:c.-336G>T
(CPLANE1)
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XP_011512392.1:n.-336G>T
|
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XM_011514092.2:c.-99G>T
(CPLANE1)
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XP_011512394.1:n.-99G>T
|
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XM_017009761.2:c.-71G>T
(CPLANE1)
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XP_016865250.1:n.-71G>T
|
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XM_017009765.1:c.-1030G>T
(CPLANE1)
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XP_016865254.1:n.-1030G>T
|
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XM_024446184.1:c.-379G>T
(CPLANE1)
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XP_024301952.1:n.-379G>T
|
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XM_024446185.1:c.-626G>T
(CPLANE1)
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XP_024301953.1:n.-626G>T
|
|
XM_024446186.1:c.-1097G>T
(CPLANE1)
|
XP_024301954.1:n.-1097G>T
|
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XR_001742208.1:n.126G>T
(CPLANE1)
|
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XR_002956171.1:n.126G>T
(CPLANE1)
|
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XR_925644.2:n.126G>T
(CPLANE1)
|
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NM_001384732.1:c.-99G>T
(CPLANE1)
MANE Select
|
NP_001371661.1:n.-99G>T
|
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NM_023073.4:c.-99G>T
(CPLANE1)
|
NP_075561.3:n.-99G>T
|
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