ENST00000281928.9:c.2707G>T
MANE Select
|
ENSP00000281928.3:p.Val903Phe
|
|
ENST00000548743.2:c.2677G>T
|
ENSP00000448553.2:p.Val893Phe
|
|
ENST00000549786.2:c.2135G>T
|
|
|
ENST00000647927.1:n.3080G>T
|
|
|
ENST00000648173.1:n.1502G>T
|
|
|
ENST00000648379.1:n.1075G>T
|
|
|
ENST00000648737.1:n.2471G>T
|
|
|
ENST00000648916.1:n.718G>T
|
|
|
ENST00000649607.1:c.891G>T
|
|
|
ENST00000650226.1:c.2707G>T
|
ENSP00000496981.1:p.Val903Phe
|
|
ENST00000281928.7:c.2707G>T
|
ENSP00000281928.3:p.Val903Phe
|
|
NM_015335.4:c.2707G>T
|
NP_056150.1:p.Val903Phe
|
|
XM_011538080.1:c.2707G>T
|
XP_011536382.1:p.Val903Phe
|
|
XM_011538081.1:c.2704G>T
|
XP_011536383.1:p.Val902Phe
|
|
XM_011538082.1:c.2677G>T
|
XP_011536384.1:p.Val893Phe
|
|
XM_011538080.2:c.2707G>T
|
XP_011536382.1:p.Val903Phe
|
|
XM_011538081.2:c.2704G>T
|
XP_011536383.1:p.Val902Phe
|
|
XM_011538082.2:c.2677G>T
|
XP_011536384.1:p.Val893Phe
|
|
XM_017019090.1:c.2704G>T
|
XP_016874579.1:p.Val902Phe
|
|
NM_015335.5:c.2707G>T
MANE Select
|
NP_056150.1:p.Val903Phe
|
|