ENST00000262494.13:c.538G>T
|
ENSP00000262494.7:p.Val180Phe
|
|
ENST00000262493.12:c.538G>T
MANE Select
|
ENSP00000262493.6:p.Val180Phe
|
|
ENST00000262494.12:c.538G>T
|
ENSP00000262494.7:p.Val180Phe
|
|
ENST00000562316.6:c.205G>T
|
ENSP00000457238.2:p.Val69Phe
|
|
ENST00000638185.1:n.753G>T
|
|
|
ENST00000638210.1:n.838G>T
|
|
|
ENST00000638705.1:c.538G>T
|
ENSP00000491223.1:p.Val180Phe
|
|
ENST00000638836.1:n.448G>T
|
|
|
ENST00000639055.1:n.1259G>T
|
|
|
ENST00000639251.1:n.439G>T
|
|
|
ENST00000639268.1:c.229-1929G>T
|
|
|
ENST00000639341.1:c.63G>T
|
|
|
ENST00000639770.1:c.576G>T
|
ENSP00000491999.1:n.576G>T
|
|
ENST00000640390.1:n.468G>T
|
|
|
ENST00000640893.1:c.377G>T
|
ENSP00000492677.1:p.Gly126Val
|
|
ENST00000262493.10:c.538G>T
|
ENSP00000262493.6:p.Val180Phe
|
|
ENST00000262494.11:c.538G>T
|
ENSP00000262494.7:p.Val180Phe
|
|
ENST00000562316.5:c.277G>T
|
ENSP00000457238.1:p.Val93Phe
|
|
NM_020988.2:c.538G>T
|
NP_066268.1:p.Val180Phe
|
|
NM_138736.2:c.538G>T
|
NP_620073.2:p.Val180Phe
|
|
XM_011523003.1:c.412G>T
|
XP_011521305.1:p.Val138Phe
|
|
XM_011523003.3:c.412G>T
|
XP_011521305.1:p.Val138Phe
|
|
NM_020988.3:c.538G>T
MANE Select
|
NP_066268.1:p.Val180Phe
|
|
NM_138736.3:c.538G>T
|
NP_620073.2:p.Val180Phe
|
|