ENST00000281928.9:c.5100G>T
MANE Select
|
ENSP00000281928.3:p.Leu1700=
|
|
ENST00000549786.2:c.4528G>T
|
|
|
ENST00000648379.1:n.3468G>T
|
|
|
ENST00000648737.1:n.4864G>T
|
|
|
ENST00000648825.1:n.1840G>T
|
|
|
ENST00000648916.1:n.3111G>T
|
|
|
ENST00000649146.1:n.2343G>T
|
|
|
ENST00000649607.1:c.3284G>T
|
|
|
ENST00000649775.1:c.1589G>T
|
|
|
ENST00000650226.1:c.5100G>T
|
ENSP00000496981.1:p.Leu1700=
|
|
ENST00000281928.7:c.5100G>T
|
ENSP00000281928.3:p.Leu1700=
|
|
ENST00000549786.1:c.464G>T
|
|
|
ENST00000552340.1:c.132G>T
|
ENSP00000449876.1:p.Leu44=
|
|
NM_015335.4:c.5100G>T
|
NP_056150.1:p.Leu1700=
|
|
XM_011538080.1:c.5100G>T
|
XP_011536382.1:p.Leu1700=
|
|
XM_011538081.1:c.5097G>T
|
XP_011536383.1:p.Leu1699=
|
|
XM_011538082.1:c.5070G>T
|
XP_011536384.1:p.Leu1690=
|
|
XM_011538080.2:c.5100G>T
|
XP_011536382.1:p.Leu1700=
|
|
XM_011538081.2:c.5097G>T
|
XP_011536383.1:p.Leu1699=
|
|
XM_011538082.2:c.5070G>T
|
XP_011536384.1:p.Leu1690=
|
|
XM_017019090.1:c.5097G>T
|
XP_016874579.1:p.Leu1699=
|
|
NM_015335.5:c.5100G>T
MANE Select
|
NP_056150.1:p.Leu1700=
|
|