ENST00000281928.9:c.2678C>G
MANE Select
|
ENSP00000281928.3:p.Thr893Arg
|
|
ENST00000548743.2:c.2648C>G
|
ENSP00000448553.2:p.Thr883Arg
|
|
ENST00000549786.2:c.2106C>G
|
|
|
ENST00000647927.1:n.3051C>G
|
|
|
ENST00000648173.1:n.1473C>G
|
|
|
ENST00000648379.1:n.1046C>G
|
|
|
ENST00000648737.1:n.2442C>G
|
|
|
ENST00000648916.1:n.689C>G
|
|
|
ENST00000649607.1:c.862C>G
|
|
|
ENST00000650226.1:c.2678C>G
|
ENSP00000496981.1:p.Thr893Arg
|
|
ENST00000281928.7:c.2678C>G
|
ENSP00000281928.3:p.Thr893Arg
|
|
NM_015335.4:c.2678C>G
|
NP_056150.1:p.Thr893Arg
|
|
XM_011538080.1:c.2678C>G
|
XP_011536382.1:p.Thr893Arg
|
|
XM_011538081.1:c.2675C>G
|
XP_011536383.1:p.Thr892Arg
|
|
XM_011538082.1:c.2648C>G
|
XP_011536384.1:p.Thr883Arg
|
|
XM_011538080.2:c.2678C>G
|
XP_011536382.1:p.Thr893Arg
|
|
XM_011538081.2:c.2675C>G
|
XP_011536383.1:p.Thr892Arg
|
|
XM_011538082.2:c.2648C>G
|
XP_011536384.1:p.Thr883Arg
|
|
XM_017019090.1:c.2675C>G
|
XP_016874579.1:p.Thr892Arg
|
|
NM_015335.5:c.2678C>G
MANE Select
|
NP_056150.1:p.Thr893Arg
|
|