ENST00000298910.12:c.4977T>A
MANE Select
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ENSP00000298910.7:p.Ala1659=
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ENST00000679360.1:c.*3886T>A
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ENSP00000505368.1:n.*3886T>A
|
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ENST00000679532.1:c.751T>A
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ENST00000680018.1:c.422T>A
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ENSP00000505347.1:n.422T>A
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ENST00000680422.1:c.622T>A
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ENST00000680425.1:c.183-897T>A
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ENSP00000506459.1:n.183-897T>A
|
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ENST00000680453.1:c.473-897T>A
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|
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ENST00000680790.1:c.4722T>A
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ENSP00000505335.1:p.Ala1574=
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ENST00000681136.1:n.961T>A
|
|
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ENST00000681696.1:c.660T>A
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ENSP00000505871.1:p.Ala220=
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ENST00000298910.11:c.4977T>A
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ENSP00000298910.7:p.Ala1659=
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ENST00000430804.5:c.2273T>A
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|
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ENST00000479187.5:n.1658T>A
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NM_198578.3:c.4977T>A
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NP_940980.3:p.Ala1659=
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XM_005268629.2:c.4977T>A
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XP_005268686.1:p.Ala1659=
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XM_011537877.1:c.4977T>A
|
XP_011536179.1:p.Ala1659=
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XM_011537878.1:c.4977T>A
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XP_011536180.1:p.Ala1659=
|
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XM_011537879.1:c.3774T>A
|
XP_011536181.1:p.Ala1258=
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XM_011537881.1:c.4828-897T>A
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XP_011536183.1:n.4828-897T>A
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XM_005268629.4:c.4977T>A
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XP_005268686.1:p.Ala1659=
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|
XM_011537877.3:c.4977T>A
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XP_011536179.1:p.Ala1659=
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XM_011537881.3:c.4828-897T>A
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XP_011536183.1:n.4828-897T>A
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XM_017018787.1:c.1893T>A
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XP_016874276.1:p.Ala631=
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XM_017018788.2:c.1239T>A
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XP_016874277.1:p.Ala413=
|
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XM_024448833.1:c.3774T>A
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XP_024304601.1:p.Ala1258=
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|
XR_001748574.2:n.5345T>A
|
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|
NM_198578.4:c.4977T>A
MANE Select
|
NP_940980.4:p.Ala1659=
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