ENST00000281928.9:c.5934G>T
MANE Select
|
ENSP00000281928.3:p.Leu1978=
|
|
ENST00000548784.2:n.2148G>T
|
|
|
ENST00000648379.1:n.4302G>T
|
|
|
ENST00000648737.1:n.5698G>T
|
|
|
ENST00000648825.1:n.4119G>T
|
|
|
ENST00000648916.1:n.3945G>T
|
|
|
ENST00000649607.1:c.4118G>T
|
|
|
ENST00000649775.1:c.2423G>T
|
|
|
ENST00000650226.1:c.5970G>T
|
ENSP00000496981.1:p.Leu1990=
|
|
ENST00000281928.7:c.5934G>T
|
ENSP00000281928.3:p.Leu1978=
|
|
ENST00000548784.1:n.432G>T
|
|
|
ENST00000552447.1:c.547G>T
|
|
|
NM_015335.4:c.5934G>T
|
NP_056150.1:p.Leu1978=
|
|
XM_011538080.1:c.5970G>T
|
XP_011536382.1:p.Leu1990=
|
|
XM_011538081.1:c.5967G>T
|
XP_011536383.1:p.Leu1989=
|
|
XM_011538082.1:c.5940G>T
|
XP_011536384.1:p.Leu1980=
|
|
XM_011538080.2:c.5970G>T
|
XP_011536382.1:p.Leu1990=
|
|
XM_011538081.2:c.5967G>T
|
XP_011536383.1:p.Leu1989=
|
|
XM_011538082.2:c.5940G>T
|
XP_011536384.1:p.Leu1980=
|
|
XM_017019090.1:c.5931G>T
|
XP_016874579.1:p.Leu1977=
|
|
NM_015335.5:c.5934G>T
MANE Select
|
NP_056150.1:p.Leu1978=
|
|