ENST00000636937.2:c.3489G>T
|
ENSP00000516154.1:p.Met1163Ile
|
|
ENST00000268124.11:c.3489G>T
MANE Select
|
ENSP00000268124.5:p.Met1163Ile
|
|
ENST00000530292.3:c.3189G>T
|
ENSP00000432885.2:n.3189G>T
|
|
ENST00000635986.2:c.*559G>T
|
ENSP00000490653.2:n.*559G>T
|
|
ENST00000636774.1:c.*2093G>T
|
ENSP00000489799.1:n.*2093G>T
|
|
ENST00000637042.1:n.72-59G>T
|
|
|
ENST00000637238.1:c.2397G>T
|
ENSP00000490756.1:n.2397G>T
|
|
ENST00000637264.1:c.2555-54G>T
|
|
|
ENST00000666746.1:c.3066G>T
|
|
|
ENST00000672071.1:n.4691G>T
|
|
|
ENST00000672695.1:n.1268G>T
|
|
|
ENST00000672923.2:n.3489G>T
|
|
|
ENST00000268124.9:c.3489G>T
|
ENSP00000268124.5:p.Met1163Ile
|
|
ENST00000442287.6:c.3489G>T
|
ENSP00000399851.2:p.Met1163Ile
|
|
ENST00000526671.1:n.299G>T
|
|
|
ENST00000530292.2:c.672G>T
|
ENSP00000432885.1:n.672G>T
|
|
ENST00000631044.2:c.*2913G>T
|
ENSP00000486730.1:n.*2913G>T
|
|
NM_001126131.1:c.3489G>T
|
NP_001119603.1:p.Met1163Ile
|
|
NM_002693.2:c.3489G>T
|
NP_002684.1:p.Met1163Ile
|
|
NM_001126131.2:c.3489G>T
|
NP_001119603.1:p.Met1163Ile
|
|
NM_002693.3:c.3489G>T
MANE Select
|
NP_002684.1:p.Met1163Ile
|
|