ENST00000706765.1:c.8774T>G
|
ENSP00000516538.1:p.Val2925Gly
|
|
ENST00000706766.1:n.1050T>G
|
|
|
ENST00000366955.8:c.8951T>G
MANE Select
|
ENSP00000355922.3:p.Val2984Gly
|
|
ENST00000366955.7:c.8951T>G
|
ENSP00000355922.3:p.Val2984Gly
|
|
ENST00000469862.1:n.722T>G
|
|
|
NM_016343.3:c.8951T>G
|
NP_057427.3:p.Val2984Gly
|
|
XM_011509082.1:c.8774T>G
|
XP_011507384.1:p.Val2925Gly
|
|
XM_011509083.1:c.7886T>G
|
XP_011507385.1:p.Val2629Gly
|
|
XM_011509082.3:c.8774T>G
|
XP_011507384.1:p.Val2925Gly
|
|
XM_017000086.2:c.8951T>G
|
XP_016855575.1:p.Val2984Gly
|
|
NM_016343.4:c.8951T>G
MANE Select
|
NP_057427.3:p.Val2984Gly
|
|