ENST00000281928.9:c.2791-1G>T
MANE Select
|
ENSP00000281928.3:n.2791-1G>T
|
|
ENST00000548743.2:c.2761-1G>T
|
ENSP00000448553.2:n.2761-1G>T
|
|
ENST00000549786.2:c.2219-1G>T
|
|
|
ENST00000647927.1:n.3164-1G>T
|
|
|
ENST00000648173.1:n.1586-1G>T
|
|
|
ENST00000648379.1:n.1159-1G>T
|
|
|
ENST00000648737.1:n.2555-1G>T
|
|
|
ENST00000648916.1:n.802-1G>T
|
|
|
ENST00000649607.1:c.975-1G>T
|
|
|
ENST00000650226.1:c.2791-1G>T
|
ENSP00000496981.1:n.2791-1G>T
|
|
ENST00000281928.7:c.2791-1G>T
|
ENSP00000281928.3:n.2791-1G>T
|
|
NM_015335.4:c.2791-1G>T
|
NP_056150.1:n.2791-1G>T
|
|
XM_011538080.1:c.2791-1G>T
|
XP_011536382.1:n.2791-1G>T
|
|
XM_011538081.1:c.2788-1G>T
|
XP_011536383.1:n.2788-1G>T
|
|
XM_011538082.1:c.2761-1G>T
|
XP_011536384.1:n.2761-1G>T
|
|
XM_011538080.2:c.2791-1G>T
|
XP_011536382.1:n.2791-1G>T
|
|
XM_011538081.2:c.2788-1G>T
|
XP_011536383.1:n.2788-1G>T
|
|
XM_011538082.2:c.2761-1G>T
|
XP_011536384.1:n.2761-1G>T
|
|
XM_017019090.1:c.2788-1G>T
|
XP_016874579.1:n.2788-1G>T
|
|
NM_015335.5:c.2791-1G>T
MANE Select
|
NP_056150.1:n.2791-1G>T
|
|