ENST00000281928.9:c.2620C>T
MANE Select
|
ENSP00000281928.3:p.His874Tyr
|
|
ENST00000548743.2:c.2590C>T
|
ENSP00000448553.2:p.His864Tyr
|
|
ENST00000549786.2:c.2048C>T
|
|
|
ENST00000647927.1:n.2993C>T
|
|
|
ENST00000648173.1:n.1415C>T
|
|
|
ENST00000648379.1:n.988C>T
|
|
|
ENST00000648737.1:n.2384C>T
|
|
|
ENST00000648916.1:n.631C>T
|
|
|
ENST00000649607.1:c.804C>T
|
|
|
ENST00000650226.1:c.2620C>T
|
ENSP00000496981.1:p.His874Tyr
|
|
ENST00000281928.7:c.2620C>T
|
ENSP00000281928.3:p.His874Tyr
|
|
NM_015335.4:c.2620C>T
|
NP_056150.1:p.His874Tyr
|
|
XM_011538080.1:c.2620C>T
|
XP_011536382.1:p.His874Tyr
|
|
XM_011538081.1:c.2617C>T
|
XP_011536383.1:p.His873Tyr
|
|
XM_011538082.1:c.2590C>T
|
XP_011536384.1:p.His864Tyr
|
|
XM_011538080.2:c.2620C>T
|
XP_011536382.1:p.His874Tyr
|
|
XM_011538081.2:c.2617C>T
|
XP_011536383.1:p.His873Tyr
|
|
XM_011538082.2:c.2590C>T
|
XP_011536384.1:p.His864Tyr
|
|
XM_017019090.1:c.2617C>T
|
XP_016874579.1:p.His873Tyr
|
|
NM_015335.5:c.2620C>T
MANE Select
|
NP_056150.1:p.His874Tyr
|
|