ENST00000295897.9:c.1476A>C
MANE Select
|
ENSP00000295897.4:p.Pro492=
|
|
ENST00000295897.8:c.1476A>C
|
ENSP00000295897.4:p.Pro492=
|
|
ENST00000401494.7:c.1131A>C
|
ENSP00000384695.3:p.Pro377=
|
|
ENST00000415165.6:c.900A>C
|
ENSP00000401820.2:p.Pro300=
|
|
ENST00000476441.6:c.*755A>C
|
ENSP00000423727.1:n.*755A>C
|
|
ENST00000486939.1:n.130A>C
|
|
|
ENST00000503124.5:c.1026A>C
|
ENSP00000421027.1:p.Pro342=
|
|
ENST00000505649.5:n.1023A>C
|
|
|
ENST00000509063.5:c.1476A>C
|
ENSP00000422784.1:p.Pro492=
|
|
ENST00000511370.1:c.1009A>C
|
|
|
ENST00000621085.4:c.837A>C
|
ENSP00000483421.1:p.Pro279=
|
|
ENST00000621628.4:c.837A>C
|
ENSP00000480485.1:p.Pro279=
|
|
NM_000477.5:c.1476A>C
|
NP_000468.1:p.Pro492=
|
|
NM_000477.6:c.1476A>C
|
NP_000468.1:p.Pro492=
|
|
NM_000477.7:c.1476A>C
MANE Select
|
NP_000468.1:p.Pro492=
|
|