ENST00000394975.3:c.382C>A
MANE Select
|
ENSP00000378426.2:p.Leu128Ile
|
|
ENST00000300851.10:c.443C>A
|
ENSP00000300851.6:p.Ala148Asp
|
|
ENST00000319788.11:c.464C>A
|
ENSP00000326135.7:p.Ala155Asp
|
|
ENST00000354895.4:c.272C>A
|
ENSP00000346969.4:p.Ala91Asp
|
|
ENST00000394971.7:c.476C>A
|
ENSP00000378422.3:p.Ala159Asp
|
|
ENST00000394975.2:c.382C>A
|
ENSP00000378426.2:p.Leu128Ile
|
|
ENST00000420057.2:c.344C>A
|
|
|
ENST00000472468.1:c.67C>A
|
ENSP00000458994.1:p.Leu23Ile
|
|
ENST00000498155.1:c.479C>A
|
ENSP00000417662.1:p.Ala160Asp
|
|
ENST00000529564.1:c.283+2068C>A
|
ENSP00000431371.1:n.283+2068C>A
|
|
ENST00000532364.1:c.173+3313C>A
|
ENSP00000460316.1:n.173+3313C>A
|
|
ENST00000533518.5:c.255C>A
|
|
|
NM_001311311.1:c.466C>A
|
NP_001298240.1:p.Leu156Ile
|
|
NM_024006.4:c.382C>A
|
NP_076869.1:p.Leu128Ile
|
|
NM_024006.5:c.382C>A
|
NP_076869.1:p.Leu128Ile
|
|
NM_206824.1:c.272C>A
|
NP_996560.1:p.Ala91Asp
|
|
NM_206824.2:c.272C>A
|
NP_996560.1:p.Ala91Asp
|
|
XM_011545944.1:c.382C>A
|
XP_011544246.1:p.Leu128Ile
|
|
XM_011545945.1:c.272C>A
|
XP_011544247.1:p.Ala91Asp
|
|
XR_950848.1:n.1170C>A
|
|
|
NM_024006.6:c.382C>A
MANE Select
|
NP_076869.1:p.Leu128Ile
|
|
NM_001311311.2:c.466C>A
|
NP_001298240.1:p.Leu156Ile
|
|
NM_206824.3:c.272C>A
|
NP_996560.1:p.Ala91Asp
|
|