ENST00000281928.9:c.3291C>A
MANE Select
|
ENSP00000281928.3:p.Pro1097=
|
|
ENST00000549786.2:c.2719C>A
|
|
|
ENST00000648379.1:n.1659C>A
|
|
|
ENST00000648737.1:n.3055C>A
|
|
|
ENST00000648825.1:n.31C>A
|
|
|
ENST00000648916.1:n.1302C>A
|
|
|
ENST00000649607.1:c.1475C>A
|
|
|
ENST00000650226.1:c.3291C>A
|
ENSP00000496981.1:p.Pro1097=
|
|
ENST00000281928.7:c.3291C>A
|
ENSP00000281928.3:p.Pro1097=
|
|
NM_015335.4:c.3291C>A
|
NP_056150.1:p.Pro1097=
|
|
XM_011538080.1:c.3291C>A
|
XP_011536382.1:p.Pro1097=
|
|
XM_011538081.1:c.3288C>A
|
XP_011536383.1:p.Pro1096=
|
|
XM_011538082.1:c.3261C>A
|
XP_011536384.1:p.Pro1087=
|
|
XM_011538080.2:c.3291C>A
|
XP_011536382.1:p.Pro1097=
|
|
XM_011538081.2:c.3288C>A
|
XP_011536383.1:p.Pro1096=
|
|
XM_011538082.2:c.3261C>A
|
XP_011536384.1:p.Pro1087=
|
|
XM_017019090.1:c.3288C>A
|
XP_016874579.1:p.Pro1096=
|
|
NM_015335.5:c.3291C>A
MANE Select
|
NP_056150.1:p.Pro1097=
|
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