ENST00000336411.7:c.1381T>C
|
ENSP00000337915.3:p.Tyr461His
|
|
ENST00000651162.1:n.723T>C
|
|
|
ENST00000651514.1:c.1288T>C
MANE Select
|
ENSP00000498939.1:p.Tyr430His
|
|
ENST00000651783.1:c.829T>C
|
ENSP00000498924.1:p.Tyr277His
|
|
ENST00000652018.1:c.1141T>C
|
ENSP00000498733.1:p.Tyr381His
|
|
ENST00000336411.6:c.1288T>C
|
ENSP00000337915.2:p.Tyr430His
|
|
ENST00000354593.6:c.838T>C
|
ENSP00000346607.2:p.Tyr280His
|
|
NM_001202855.2:c.1285T>C
|
NP_001189784.1:p.Tyr429His
|
|
NM_017460.5:c.1288T>C
|
NP_059488.2:p.Tyr430His
|
|
XM_011515841.1:c.1381T>C
|
XP_011514143.1:p.Tyr461His
|
|
XM_011515842.1:c.1378T>C
|
XP_011514144.1:p.Tyr460His
|
|
NM_017460.6:c.1288T>C
MANE Select
|
NP_059488.2:p.Tyr430His
|
|
NM_001202855.3:c.1285T>C
|
NP_001189784.1:p.Tyr429His
|
|