ENST00000368985.8:c.936G>T
MANE Select
|
ENSP00000357981.3:p.Met312Ile
|
|
ENST00000448301.7:c.708G>T
|
ENSP00000408414.2:p.Met236Ile
|
|
ENST00000472977.7:c.936G>T
|
ENSP00000475176.2:p.Met312Ile
|
|
ENST00000483930.2:c.*130G>T
|
ENSP00000475812.2:n.*130G>T
|
|
ENST00000607427.2:c.936G>T
|
ENSP00000475557.2:p.Met312Ile
|
|
ENST00000679512.1:c.833G>T
|
ENSP00000505113.1:p.Trp278Leu
|
|
ENST00000679898.1:c.663G>T
|
ENSP00000505326.1:p.Met221Ile
|
|
ENST00000680288.1:c.786G>T
|
ENSP00000506001.1:p.Met262Ile
|
|
ENST00000680311.1:c.*19G>T
|
ENSP00000505020.1:n.*19G>T
|
|
ENST00000680471.1:c.*107G>T
|
ENSP00000506603.1:n.*107G>T
|
|
ENST00000680664.1:c.759G>T
|
ENSP00000506248.1:p.Met253Ile
|
|
ENST00000680931.1:c.*286G>T
|
ENSP00000504934.1:n.*286G>T
|
|
ENST00000681357.1:n.326G>T
|
|
|
ENST00000681444.1:c.936G>T
|
ENSP00000505359.1:p.Met312Ile
|
|
ENST00000368985.7:c.936G>T
|
ENSP00000357981.3:p.Met312Ile
|
|
ENST00000448301.6:c.786G>T
|
ENSP00000408414.1:p.Met262Ile
|
|
ENST00000472977.6:c.229G>T
|
|
|
ENST00000483930.1:c.484G>T
|
ENSP00000475812.1:n.484G>T
|
|
NM_001199739.1:c.786G>T
|
NP_001186668.1:p.Met262Ile
|
|
NM_004079.4:c.936G>T
|
NP_004070.3:p.Met312Ile
|
|
NM_004079.5:c.936G>T
MANE Select
|
NP_004070.3:p.Met312Ile
|
|
NM_001199739.2:c.786G>T
|
NP_001186668.1:p.Met262Ile
|
|