ENST00000368985.8:c.934A>C
MANE Select
|
ENSP00000357981.3:p.Met312Leu
|
|
ENST00000448301.7:c.706A>C
|
ENSP00000408414.2:p.Met236Leu
|
|
ENST00000472977.7:c.934A>C
|
ENSP00000475176.2:p.Met312Leu
|
|
ENST00000483930.2:c.*128A>C
|
ENSP00000475812.2:n.*128A>C
|
|
ENST00000607427.2:c.934A>C
|
ENSP00000475557.2:p.Met312Leu
|
|
ENST00000679512.1:c.831A>C
|
ENSP00000505113.1:p.Gly277=
|
|
ENST00000679898.1:c.661A>C
|
ENSP00000505326.1:p.Met221Leu
|
|
ENST00000680288.1:c.784A>C
|
ENSP00000506001.1:p.Met262Leu
|
|
ENST00000680311.1:c.*17A>C
|
ENSP00000505020.1:n.*17A>C
|
|
ENST00000680471.1:c.*105A>C
|
ENSP00000506603.1:n.*105A>C
|
|
ENST00000680664.1:c.757A>C
|
ENSP00000506248.1:p.Met253Leu
|
|
ENST00000680931.1:c.*284A>C
|
ENSP00000504934.1:n.*284A>C
|
|
ENST00000681357.1:n.324A>C
|
|
|
ENST00000681444.1:c.934A>C
|
ENSP00000505359.1:p.Met312Leu
|
|
ENST00000368985.7:c.934A>C
|
ENSP00000357981.3:p.Met312Leu
|
|
ENST00000448301.6:c.784A>C
|
ENSP00000408414.1:p.Met262Leu
|
|
ENST00000472977.6:c.227A>C
|
|
|
ENST00000483930.1:c.482A>C
|
ENSP00000475812.1:n.482A>C
|
|
NM_001199739.1:c.784A>C
|
NP_001186668.1:p.Met262Leu
|
|
NM_004079.4:c.934A>C
|
NP_004070.3:p.Met312Leu
|
|
NM_004079.5:c.934A>C
MANE Select
|
NP_004070.3:p.Met312Leu
|
|
NM_001199739.2:c.784A>C
|
NP_001186668.1:p.Met262Leu
|
|