ENST00000281928.9:c.3276C>T
MANE Select
|
ENSP00000281928.3:p.Leu1092=
|
|
ENST00000549786.2:c.2704C>T
|
|
|
ENST00000648379.1:n.1644C>T
|
|
|
ENST00000648737.1:n.3040C>T
|
|
|
ENST00000648825.1:n.16C>T
|
|
|
ENST00000648916.1:n.1287C>T
|
|
|
ENST00000649607.1:c.1460C>T
|
|
|
ENST00000650226.1:c.3276C>T
|
ENSP00000496981.1:p.Leu1092=
|
|
ENST00000281928.7:c.3276C>T
|
ENSP00000281928.3:p.Leu1092=
|
|
NM_015335.4:c.3276C>T
|
NP_056150.1:p.Leu1092=
|
|
XM_011538080.1:c.3276C>T
|
XP_011536382.1:p.Leu1092=
|
|
XM_011538081.1:c.3273C>T
|
XP_011536383.1:p.Leu1091=
|
|
XM_011538082.1:c.3246C>T
|
XP_011536384.1:p.Leu1082=
|
|
XM_011538080.2:c.3276C>T
|
XP_011536382.1:p.Leu1092=
|
|
XM_011538081.2:c.3273C>T
|
XP_011536383.1:p.Leu1091=
|
|
XM_011538082.2:c.3246C>T
|
XP_011536384.1:p.Leu1082=
|
|
XM_017019090.1:c.3273C>T
|
XP_016874579.1:p.Leu1091=
|
|
NM_015335.5:c.3276C>T
MANE Select
|
NP_056150.1:p.Leu1092=
|
|