|
ENST00000703936.1:c.2695G>T
|
ENSP00000515567.1:p.Val899Leu
|
|
|
ENST00000703937.1:c.*1756G>T
|
ENSP00000515568.1:n.*1756G>T
|
|
|
ENST00000326739.9:c.655G>T
MANE Select
|
ENSP00000321584.4:p.Val219Leu
|
|
|
ENST00000429182.6:c.655G>T
|
ENSP00000393525.2:p.Val219Leu
|
|
|
ENST00000442157.2:c.580G>T
|
ENSP00000403502.2:p.Val194Leu
|
|
|
ENST00000462980.2:n.1170G>T
|
|
|
|
ENST00000472328.2:n.721G>T
|
|
|
|
ENST00000491610.2:n.615G>T
|
|
|
|
ENST00000676607.1:n.951G>T
|
|
|
|
ENST00000676627.1:n.1385G>T
|
|
|
|
ENST00000676708.1:n.1935G>T
|
|
|
|
ENST00000676864.1:n.1804G>T
|
|
|
|
ENST00000677010.1:c.691G>T
|
ENSP00000503089.1:p.Val231Leu
|
|
|
ENST00000677108.1:n.2561G>T
|
|
|
|
ENST00000677168.1:n.1127G>T
|
|
|
|
ENST00000677185.1:n.1218G>T
|
|
|
|
ENST00000677205.1:n.1439G>T
|
|
|
|
ENST00000677344.1:n.1929G>T
|
|
|
|
ENST00000677480.1:c.*332G>T
|
ENSP00000504378.1:n.*332G>T
|
|
|
ENST00000677519.1:n.1365G>T
|
|
|
|
ENST00000677593.1:n.1211G>T
|
|
|
|
ENST00000677740.1:n.2160G>T
|
|
|
|
ENST00000677991.1:n.1828G>T
|
|
|
|
ENST00000678001.1:n.1148G>T
|
|
|
|
ENST00000678085.1:n.1211G>T
|
|
|
|
ENST00000678177.1:n.2504G>T
|
|
|
|
ENST00000678603.1:n.1733G>T
|
|
|
|
ENST00000678724.1:c.580G>T
|
ENSP00000503874.1:p.Val194Leu
|
|
|
ENST00000678920.1:n.813G>T
|
|
|
|
ENST00000679019.1:n.1425G>T
|
|
|
|
ENST00000679117.1:c.*470G>T
|
ENSP00000503240.1:n.*470G>T
|
|
|
ENST00000679339.1:n.1496G>T
|
|
|
|
ENST00000326739.8:c.655G>T
|
ENSP00000321584.4:p.Val219Leu
|
|
|
ENST00000429182.5:c.449G>T
|
|
|
|
ENST00000442157.1:c.580G>T
|
ENSP00000403502.1:p.Val194Leu
|
|
|
ENST00000462980.1:n.557G>T
|
|
|
|
ENST00000491610.1:n.615G>T
|
|
|
|
NM_000884.2:c.655G>T
|
NP_000875.2:p.Val219Leu
|
|
|
XM_006713128.2:c.865G>T
|
XP_006713191.1:p.Val289Leu
|
|
|
XM_006713128.3:c.865G>T
|
XP_006713191.1:p.Val289Leu
|
|
|
XM_017006349.1:c.790G>T
|
XP_016861838.1:p.Val264Leu
|
|
|
XM_017006350.1:c.790G>T
|
XP_016861839.1:p.Val264Leu
|
|
|
NM_000884.3:c.655G>T
MANE Select
|
NP_000875.2:p.Val219Leu
|
|
