ENST00000706765.1:c.8611G>C
|
ENSP00000516538.1:p.Gly2871Arg
|
|
ENST00000706766.1:n.887G>C
|
|
|
ENST00000366955.8:c.8788G>C
MANE Select
|
ENSP00000355922.3:p.Gly2930Arg
|
|
ENST00000366955.7:c.8788G>C
|
ENSP00000355922.3:p.Gly2930Arg
|
|
ENST00000469862.1:n.559G>C
|
|
|
NM_016343.3:c.8788G>C
|
NP_057427.3:p.Gly2930Arg
|
|
XM_011509082.1:c.8611G>C
|
XP_011507384.1:p.Gly2871Arg
|
|
XM_011509083.1:c.7723G>C
|
XP_011507385.1:p.Gly2575Arg
|
|
XM_011509082.3:c.8611G>C
|
XP_011507384.1:p.Gly2871Arg
|
|
XM_017000086.2:c.8788G>C
|
XP_016855575.1:p.Gly2930Arg
|
|
NM_016343.4:c.8788G>C
MANE Select
|
NP_057427.3:p.Gly2930Arg
|
|