ENST00000299314.12:c.508G>T
MANE Select
|
ENSP00000299314.7:p.Val170Phe
|
|
ENST00000299314.11:c.508G>T
|
ENSP00000299314.7:p.Val170Phe
|
|
ENST00000549940.5:c.508G>T
|
ENSP00000449150.1:p.Val170Phe
|
|
ENST00000550352.1:n.302G>T
|
|
|
ENST00000552681.1:c.142G>T
|
ENSP00000449217.1:p.Val48Phe
|
|
NM_024312.4:c.508G>T
|
NP_077288.2:p.Val170Phe
|
|
XM_006719593.2:c.508G>T
|
XP_006719656.1:p.Val170Phe
|
|
XM_011538731.1:c.427G>T
|
XP_011537033.1:p.Val143Phe
|
|
XM_006719593.3:c.508G>T
|
XP_006719656.1:p.Val170Phe
|
|
XM_011538731.2:c.427G>T
|
XP_011537033.1:p.Val143Phe
|
|
XM_017019961.1:c.292G>T
|
XP_016875450.1:p.Val98Phe
|
|
XM_017019962.2:c.-843G>T
|
XP_016875451.1:n.-843G>T
|
|
NM_024312.5:c.508G>T
MANE Select
|
NP_077288.2:p.Val170Phe
|
|