ENST00000336411.7:c.1408C>G
|
ENSP00000337915.3:p.Pro470Ala
|
|
ENST00000651162.1:n.750C>G
|
|
|
ENST00000651514.1:c.1315C>G
MANE Select
|
ENSP00000498939.1:p.Pro439Ala
|
|
ENST00000651783.1:c.856C>G
|
ENSP00000498924.1:p.Pro286Ala
|
|
ENST00000652018.1:c.1168C>G
|
ENSP00000498733.1:p.Pro390Ala
|
|
ENST00000336411.6:c.1315C>G
|
ENSP00000337915.2:p.Pro439Ala
|
|
ENST00000354593.6:c.865C>G
|
ENSP00000346607.2:p.Pro289Ala
|
|
NM_001202855.2:c.1312C>G
|
NP_001189784.1:p.Pro438Ala
|
|
NM_017460.5:c.1315C>G
|
NP_059488.2:p.Pro439Ala
|
|
XM_011515841.1:c.1408C>G
|
XP_011514143.1:p.Pro470Ala
|
|
XM_011515842.1:c.1405C>G
|
XP_011514144.1:p.Pro469Ala
|
|
NM_017460.6:c.1315C>G
MANE Select
|
NP_059488.2:p.Pro439Ala
|
|
NM_001202855.3:c.1312C>G
|
NP_001189784.1:p.Pro438Ala
|
|