ENST00000422737.7:c.4696G>T
|
ENSP00000415650.3:p.Ala1566Ser
|
|
ENST00000457135.2:c.905G>T
|
|
|
ENST00000334344.11:c.4696G>T
MANE Select
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ENSP00000335044.6:p.Ala1566Ser
|
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ENST00000422737.6:c.4617G>T
|
|
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ENST00000334344.10:c.4696G>T
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ENSP00000335044.6:p.Ala1566Ser
|
|
ENST00000422737.5:c.4249G>T
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ENSP00000415650.1:p.Ala1417Ser
|
|
ENST00000444670.5:c.3526G>T
|
ENSP00000397307.1:p.Ala1176Ser
|
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ENST00000457135.1:c.520G>T
|
ENSP00000388357.1:p.Ala174Ser
|
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ENST00000479608.5:n.3987G>T
|
|
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NM_152641.2:c.4696G>T
|
NP_689854.2:p.Ala1566Ser
|
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XM_006719272.2:c.4696G>T
|
XP_006719335.1:p.Ala1566Ser
|
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XM_011538025.1:c.3064G>T
|
XP_011536327.1:p.Ala1022Ser
|
|
XR_944505.1:n.4844G>T
|
|
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NM_001347839.1:c.4696G>T
|
NP_001334768.1:p.Ala1566Ser
|
|
NM_152641.3:c.4696G>T
|
NP_689854.2:p.Ala1566Ser
|
|
XM_006719272.4:c.4696G>T
|
XP_006719335.1:p.Ala1566Ser
|
|
XR_944505.3:n.4827G>T
|
|
|
NM_152641.4:c.4696G>T
MANE Select
|
NP_689854.2:p.Ala1566Ser
|
|
NM_001347839.2:c.4696G>T
|
NP_001334768.1:p.Ala1566Ser
|
|