ENST00000706765.1:c.8702C>T
|
ENSP00000516538.1:p.Ala2901Val
|
|
ENST00000706766.1:n.978C>T
|
|
|
ENST00000366955.8:c.8879C>T
MANE Select
|
ENSP00000355922.3:p.Ala2960Val
|
|
ENST00000366955.7:c.8879C>T
|
ENSP00000355922.3:p.Ala2960Val
|
|
ENST00000469862.1:n.650C>T
|
|
|
NM_016343.3:c.8879C>T
|
NP_057427.3:p.Ala2960Val
|
|
XM_011509082.1:c.8702C>T
|
XP_011507384.1:p.Ala2901Val
|
|
XM_011509083.1:c.7814C>T
|
XP_011507385.1:p.Ala2605Val
|
|
XM_011509082.3:c.8702C>T
|
XP_011507384.1:p.Ala2901Val
|
|
XM_017000086.2:c.8879C>T
|
XP_016855575.1:p.Ala2960Val
|
|
NM_016343.4:c.8879C>T
MANE Select
|
NP_057427.3:p.Ala2960Val
|
|