ENST00000474381.2:n.2929C>A
|
|
|
ENST00000481849.6:n.2355C>A
|
|
|
ENST00000497377.6:n.2355C>A
|
|
|
ENST00000640094.2:c.882C>A
|
ENSP00000491275.2:p.Leu294=
|
|
ENST00000696558.1:c.951C>A
|
ENSP00000512716.1:n.951C>A
|
|
ENST00000696559.1:c.882C>A
|
ENSP00000512717.1:p.Leu294=
|
|
ENST00000696560.1:c.882C>A
|
ENSP00000512718.1:p.Leu294=
|
|
ENST00000696561.1:c.882C>A
|
ENSP00000512719.1:p.Leu294=
|
|
ENST00000696562.1:c.882C>A
|
ENSP00000512720.1:p.Leu294=
|
|
ENST00000412585.7:c.882C>A
MANE Select
|
ENSP00000399168.2:p.Leu294=
|
|
ENST00000640094.1:c.75C>A
|
ENSP00000491275.1:p.Leu25=
|
|
ENST00000412585.6:c.882C>A
|
ENSP00000399168.2:p.Leu294=
|
|
ENST00000463574.1:n.473C>A
|
|
|
NM_005514.6:c.882C>A
|
NP_005505.2:p.Leu294=
|
|
XM_011514556.1:c.915C>A
|
XP_011512858.1:p.Leu305=
|
|
XM_011514557.1:c.882C>A
|
XP_011512859.1:p.Leu294=
|
|
XR_926175.1:n.1321C>A
|
|
|
NM_005514.7:c.882C>A
|
NP_005505.2:p.Leu294=
|
|
NM_005514.8:c.882C>A
MANE Select
|
NP_005505.2:p.Leu294=
|
|