ENST00000553591.2:c.702G>A
|
ENSP00000452421.2:p.Val234=
|
|
ENST00000556293.6:n.3008G>A
|
|
|
ENST00000556754.2:n.3951G>A
|
|
|
ENST00000557229.6:n.1014G>A
|
|
|
ENST00000697613.1:c.585G>A
|
ENSP00000513359.1:p.Val195=
|
|
ENST00000697614.1:c.348G>A
|
ENSP00000513360.1:p.Val116=
|
|
ENST00000697615.1:n.1413G>A
|
|
|
ENST00000361505.10:c.585G>A
MANE Select
|
ENSP00000354532.6:p.Val195=
|
|
ENST00000361505.9:c.585G>A
|
ENSP00000354532.5:p.Val195=
|
|
ENST00000554056.5:n.893G>A
|
|
|
ENST00000556754.1:n.1802G>A
|
|
|
NM_000270.3:c.585G>A , LRG_91t1:c.585G>A
|
NP_000261.2:p.Val195=
|
|
NM_000270.4:c.585G>A
MANE Select
|
NP_000261.2:p.Val195=
|
|