ENST00000336411.7:c.1379C>A
|
ENSP00000337915.3:p.Pro460His
|
|
ENST00000651162.1:n.721C>A
|
|
|
ENST00000651514.1:c.1286C>A
MANE Select
|
ENSP00000498939.1:p.Pro429His
|
|
ENST00000651783.1:c.827C>A
|
ENSP00000498924.1:p.Pro276His
|
|
ENST00000652018.1:c.1139C>A
|
ENSP00000498733.1:p.Pro380His
|
|
ENST00000336411.6:c.1286C>A
|
ENSP00000337915.2:p.Pro429His
|
|
ENST00000354593.6:c.836C>A
|
ENSP00000346607.2:p.Pro279His
|
|
NM_001202855.2:c.1283C>A
|
NP_001189784.1:p.Pro428His
|
|
NM_017460.5:c.1286C>A
|
NP_059488.2:p.Pro429His
|
|
XM_011515841.1:c.1379C>A
|
XP_011514143.1:p.Pro460His
|
|
XM_011515842.1:c.1376C>A
|
XP_011514144.1:p.Pro459His
|
|
NM_017460.6:c.1286C>A
MANE Select
|
NP_059488.2:p.Pro429His
|
|
NM_001202855.3:c.1283C>A
|
NP_001189784.1:p.Pro428His
|
|