ENST00000703783.1:n.996C>T
|
|
|
ENST00000703785.1:n.1077C>T
|
|
|
ENST00000262464.9:c.4212C>T
MANE Select
|
ENSP00000262464.4:p.Ile1404=
|
|
ENST00000262464.8:c.4212C>T
|
ENSP00000262464.4:p.Ile1404=
|
|
ENST00000507835.5:c.762C>T
|
ENSP00000426839.1:p.Ile254=
|
|
ENST00000508053.5:c.4212C>T
|
ENSP00000424571.1:p.Ile1404=
|
|
ENST00000508989.5:c.4113C>T
|
ENSP00000425596.1:p.Ile1371=
|
|
ENST00000619499.4:c.4209C>T
|
ENSP00000482132.1:p.Ile1403=
|
|
NM_001999.3:c.4212C>T
|
NP_001990.2:p.Ile1404=
|
|
XM_017009228.2:c.4059C>T
|
XP_016864717.1:p.Ile1353=
|
|
NM_001999.4:c.4212C>T
MANE Select
|
NP_001990.2:p.Ile1404=
|
|