ENST00000291295.14:c.231G>T
MANE Select
|
ENSP00000291295.8:p.Met77Ile
|
|
ENST00000595072.2:n.2660G>T
|
|
|
ENST00000602169.2:c.*267G>T
|
ENSP00000499372.1:n.*267G>T
|
|
ENST00000291295.13:c.231G>T
|
ENSP00000291295.8:p.Met77Ile
|
|
ENST00000391918.6:c.123G>T
|
ENSP00000375785.2:p.Met41Ile
|
|
ENST00000477244.5:n.355G>T
|
|
|
ENST00000482455.5:n.341G>T
|
|
|
ENST00000486500.1:n.432G>T
|
|
|
ENST00000594523.5:c.123G>T
|
ENSP00000468877.1:p.Met41Ile
|
|
ENST00000595072.1:n.421G>T
|
|
|
ENST00000596362.1:c.231G>T
|
ENSP00000472141.1:p.Met77Ile
|
|
ENST00000597743.5:c.165+207G>T
|
ENSP00000470308.1:n.165+207G>T
|
|
ENST00000597868.5:n.299G>T
|
|
|
ENST00000598871.5:c.123G>T
|
ENSP00000470502.1:p.Met41Ile
|
|
ENST00000599839.5:c.123G>T
|
ENSP00000471225.1:p.Met41Ile
|
|
NM_005184.2:c.231G>T
|
NP_005175.2:p.Met77Ile
|
|
NM_001329921.1:c.123G>T
|
NP_001316850.1:p.Met41Ile
|
|
NM_001329922.1:c.231G>T
|
NP_001316851.1:p.Met77Ile
|
|
NM_001329923.1:c.123G>T
|
NP_001316852.1:p.Met41Ile
|
|
NM_001329924.1:c.123G>T
|
NP_001316853.1:p.Met41Ile
|
|
NM_001329925.1:c.123G>T
|
NP_001316854.1:p.Met41Ile
|
|
NM_001329926.1:c.123G>T
|
NP_001316855.1:p.Met41Ile
|
|
NM_005184.3:c.231G>T
|
NP_005175.2:p.Met77Ile
|
|
NM_001329924.2:c.123G>T
|
NP_001316853.1:p.Met41Ile
|
|
NM_001329925.2:c.123G>T
|
NP_001316854.1:p.Met41Ile
|
|
NM_001329926.2:c.123G>T
|
NP_001316855.1:p.Met41Ile
|
|
NM_005184.4:c.231G>T
MANE Select
|
NP_005175.2:p.Met77Ile
|
|