ENST00000295897.9:c.1456G>T
MANE Select
|
ENSP00000295897.4:p.Val486Leu
|
|
ENST00000295897.8:c.1456G>T
|
ENSP00000295897.4:p.Val486Leu
|
|
ENST00000401494.7:c.1111G>T
|
ENSP00000384695.3:p.Val371Leu
|
|
ENST00000415165.6:c.880G>T
|
ENSP00000401820.2:p.Val294Leu
|
|
ENST00000476441.6:c.*735G>T
|
ENSP00000423727.1:n.*735G>T
|
|
ENST00000486939.1:n.110G>T
|
|
|
ENST00000503124.5:c.1006G>T
|
ENSP00000421027.1:p.Val336Leu
|
|
ENST00000505649.5:n.1003G>T
|
|
|
ENST00000509063.5:c.1456G>T
|
ENSP00000422784.1:p.Val486Leu
|
|
ENST00000511370.1:c.989G>T
|
|
|
ENST00000621085.4:c.817G>T
|
ENSP00000483421.1:p.Val273Leu
|
|
ENST00000621628.4:c.817G>T
|
ENSP00000480485.1:p.Val273Leu
|
|
NM_000477.5:c.1456G>T
|
NP_000468.1:p.Val486Leu
|
|
NM_000477.6:c.1456G>T
|
NP_000468.1:p.Val486Leu
|
|
NM_000477.7:c.1456G>T
MANE Select
|
NP_000468.1:p.Val486Leu
|
|