ENST00000299314.12:c.538G>T
MANE Select
|
ENSP00000299314.7:p.Val180Phe
|
|
ENST00000299314.11:c.538G>T
|
ENSP00000299314.7:p.Val180Phe
|
|
ENST00000549940.5:c.538G>T
|
ENSP00000449150.1:p.Val180Phe
|
|
ENST00000550352.1:n.332G>T
|
|
|
ENST00000552681.1:c.172G>T
|
ENSP00000449217.1:p.Val58Phe
|
|
NM_024312.4:c.538G>T
|
NP_077288.2:p.Val180Phe
|
|
XM_006719593.2:c.538G>T
|
XP_006719656.1:p.Val180Phe
|
|
XM_011538731.1:c.457G>T
|
XP_011537033.1:p.Val153Phe
|
|
XM_006719593.3:c.538G>T
|
XP_006719656.1:p.Val180Phe
|
|
XM_011538731.2:c.457G>T
|
XP_011537033.1:p.Val153Phe
|
|
XM_017019961.1:c.322G>T
|
XP_016875450.1:p.Val108Phe
|
|
XM_017019962.2:c.-813G>T
|
XP_016875451.1:n.-813G>T
|
|
NM_024312.5:c.538G>T
MANE Select
|
NP_077288.2:p.Val180Phe
|
|