ENST00000336411.7:c.1382A>G
|
ENSP00000337915.3:p.Tyr461Cys
|
|
ENST00000651162.1:n.724A>G
|
|
|
ENST00000651514.1:c.1289A>G
MANE Select
|
ENSP00000498939.1:p.Tyr430Cys
|
|
ENST00000651783.1:c.830A>G
|
ENSP00000498924.1:p.Tyr277Cys
|
|
ENST00000652018.1:c.1142A>G
|
ENSP00000498733.1:p.Tyr381Cys
|
|
ENST00000336411.6:c.1289A>G
|
ENSP00000337915.2:p.Tyr430Cys
|
|
ENST00000354593.6:c.839A>G
|
ENSP00000346607.2:p.Tyr280Cys
|
|
NM_001202855.2:c.1286A>G
|
NP_001189784.1:p.Tyr429Cys
|
|
NM_017460.5:c.1289A>G
|
NP_059488.2:p.Tyr430Cys
|
|
XM_011515841.1:c.1382A>G
|
XP_011514143.1:p.Tyr461Cys
|
|
XM_011515842.1:c.1379A>G
|
XP_011514144.1:p.Tyr460Cys
|
|
NM_017460.6:c.1289A>G
MANE Select
|
NP_059488.2:p.Tyr430Cys
|
|
NM_001202855.3:c.1286A>G
|
NP_001189784.1:p.Tyr429Cys
|
|