ENST00000290866.10:c.3731G>T
MANE Select
|
ENSP00000290866.4:p.Ser1244Ile
|
|
ENST00000290863.10:c.2009G>T
|
ENSP00000290863.6:p.Ser670Ile
|
|
ENST00000290866.9:c.3731G>T
|
ENSP00000290866.4:p.Ser1244Ile
|
|
ENST00000413513.7:c.1886G>T
|
ENSP00000392247.3:p.Ser629Ile
|
|
ENST00000428043.5:c.*153G>T
|
ENSP00000397593.2:n.*153G>T
|
|
ENST00000577647.2:c.1969+191G>T
|
ENSP00000464149.1:n.1969+191G>T
|
|
ENST00000578839.5:c.*1486G>T
|
ENSP00000462110.2:n.*1486G>T
|
|
ENST00000579314.5:c.*1460G>T
|
ENSP00000462599.1:n.*1460G>T
|
|
NM_000789.3:c.3731G>T
|
NP_000780.1:p.Ser1244Ile
|
|
NM_001178057.1:c.1886G>T
|
NP_001171528.1:p.Ser629Ile
|
|
NM_152830.2:c.2009G>T
|
NP_690043.1:p.Ser670Ile
|
|
XM_005257110.1:c.3182G>T
|
XP_005257167.1:p.Ser1061Ile
|
|
XM_006721737.2:c.2069G>T
|
XP_006721800.2:p.Ser690Ile
|
|
XM_006721737.3:c.2069G>T
|
XP_006721800.2:p.Ser690Ile
|
|
NM_000789.4:c.3731G>T
MANE Select
|
NP_000780.1:p.Ser1244Ile
|
|
NM_001178057.2:c.1886G>T
|
NP_001171528.1:p.Ser629Ile
|
|
NM_152830.3:c.2009G>T
|
NP_690043.1:p.Ser670Ile
|
|
NM_001382700.1:c.3164G>T
|
NP_001369629.1:p.Ser1055Ile
|
|
NM_001382701.1:c.2879G>T
|
NP_001369630.1:p.Ser960Ile
|
|
NM_001382702.1:c.1346G>T
|
NP_001369631.1:p.Ser449Ile
|
|
NR_168483.1:n.2109G>T
|
|
|