ENST00000368985.8:c.965T>G
MANE Select
|
ENSP00000357981.3:p.Ile322Ser
|
|
ENST00000448301.7:c.737T>G
|
ENSP00000408414.2:p.Ile246Ser
|
|
ENST00000472977.7:c.965T>G
|
ENSP00000475176.2:p.Ile322Ser
|
|
ENST00000483930.2:c.*159T>G
|
ENSP00000475812.2:n.*159T>G
|
|
ENST00000607427.2:c.965T>G
|
ENSP00000475557.2:p.Ile322Ser
|
|
ENST00000679512.1:c.862T>G
|
ENSP00000505113.1:p.Leu288Val
|
|
ENST00000679898.1:c.692T>G
|
ENSP00000505326.1:p.Ile231Ser
|
|
ENST00000680288.1:c.815T>G
|
ENSP00000506001.1:p.Ile272Ser
|
|
ENST00000680311.1:c.*48T>G
|
ENSP00000505020.1:n.*48T>G
|
|
ENST00000680471.1:c.*136T>G
|
ENSP00000506603.1:n.*136T>G
|
|
ENST00000680664.1:c.788T>G
|
ENSP00000506248.1:p.Ile263Ser
|
|
ENST00000680931.1:c.*315T>G
|
ENSP00000504934.1:n.*315T>G
|
|
ENST00000681357.1:n.355T>G
|
|
|
ENST00000681444.1:c.965T>G
|
ENSP00000505359.1:p.Ile322Ser
|
|
ENST00000368985.7:c.965T>G
|
ENSP00000357981.3:p.Ile322Ser
|
|
ENST00000448301.6:c.815T>G
|
ENSP00000408414.1:p.Ile272Ser
|
|
ENST00000472977.6:c.258T>G
|
|
|
ENST00000483930.1:c.513T>G
|
ENSP00000475812.1:n.513T>G
|
|
NM_001199739.1:c.815T>G
|
NP_001186668.1:p.Ile272Ser
|
|
NM_004079.4:c.965T>G
|
NP_004070.3:p.Ile322Ser
|
|
NM_004079.5:c.965T>G
MANE Select
|
NP_004070.3:p.Ile322Ser
|
|
NM_001199739.2:c.815T>G
|
NP_001186668.1:p.Ile272Ser
|
|