ENST00000281928.9:c.4988C>G
MANE Select
|
ENSP00000281928.3:p.Thr1663Arg
|
|
ENST00000549786.2:c.4416C>G
|
|
|
ENST00000648379.1:n.3356C>G
|
|
|
ENST00000648737.1:n.4752C>G
|
|
|
ENST00000648825.1:n.1728C>G
|
|
|
ENST00000648916.1:n.2999C>G
|
|
|
ENST00000649146.1:n.2231C>G
|
|
|
ENST00000649607.1:c.3172C>G
|
|
|
ENST00000649775.1:c.1477C>G
|
|
|
ENST00000650226.1:c.4988C>G
|
ENSP00000496981.1:p.Thr1663Arg
|
|
ENST00000281928.7:c.4988C>G
|
ENSP00000281928.3:p.Thr1663Arg
|
|
ENST00000549786.1:c.352C>G
|
|
|
ENST00000552340.1:c.20C>G
|
ENSP00000449876.1:p.Thr7Arg
|
|
NM_015335.4:c.4988C>G
|
NP_056150.1:p.Thr1663Arg
|
|
XM_011538080.1:c.4988C>G
|
XP_011536382.1:p.Thr1663Arg
|
|
XM_011538081.1:c.4985C>G
|
XP_011536383.1:p.Thr1662Arg
|
|
XM_011538082.1:c.4958C>G
|
XP_011536384.1:p.Thr1653Arg
|
|
XM_011538080.2:c.4988C>G
|
XP_011536382.1:p.Thr1663Arg
|
|
XM_011538081.2:c.4985C>G
|
XP_011536383.1:p.Thr1662Arg
|
|
XM_011538082.2:c.4958C>G
|
XP_011536384.1:p.Thr1653Arg
|
|
XM_017019090.1:c.4985C>G
|
XP_016874579.1:p.Thr1662Arg
|
|
NM_015335.5:c.4988C>G
MANE Select
|
NP_056150.1:p.Thr1663Arg
|
|