|
ENST00000703936.1:c.2753A>C
|
ENSP00000515567.1:p.Lys918Thr
|
|
|
ENST00000703937.1:c.*1814A>C
|
ENSP00000515568.1:n.*1814A>C
|
|
|
ENST00000326739.9:c.713A>C
MANE Select
|
ENSP00000321584.4:p.Lys238Thr
|
|
|
ENST00000429182.6:c.713A>C
|
ENSP00000393525.2:p.Lys238Thr
|
|
|
ENST00000442157.2:c.638A>C
|
ENSP00000403502.2:p.Lys213Thr
|
|
|
ENST00000462980.2:n.1228A>C
|
|
|
|
ENST00000472328.2:n.779A>C
|
|
|
|
ENST00000491610.2:n.673A>C
|
|
|
|
ENST00000676607.1:n.1009A>C
|
|
|
|
ENST00000676627.1:n.1443A>C
|
|
|
|
ENST00000676708.1:n.1993A>C
|
|
|
|
ENST00000676864.1:n.1862A>C
|
|
|
|
ENST00000677010.1:c.749A>C
|
ENSP00000503089.1:p.Lys250Thr
|
|
|
ENST00000677108.1:n.2619A>C
|
|
|
|
ENST00000677168.1:n.1185A>C
|
|
|
|
ENST00000677185.1:n.1276A>C
|
|
|
|
ENST00000677205.1:n.1497A>C
|
|
|
|
ENST00000677344.1:n.1987A>C
|
|
|
|
ENST00000677480.1:c.*390A>C
|
ENSP00000504378.1:n.*390A>C
|
|
|
ENST00000677519.1:n.1423A>C
|
|
|
|
ENST00000677593.1:n.1269A>C
|
|
|
|
ENST00000677740.1:n.2218A>C
|
|
|
|
ENST00000677991.1:n.1886A>C
|
|
|
|
ENST00000678001.1:n.1206A>C
|
|
|
|
ENST00000678085.1:n.1269A>C
|
|
|
|
ENST00000678177.1:n.2562A>C
|
|
|
|
ENST00000678603.1:n.1791A>C
|
|
|
|
ENST00000678724.1:c.638A>C
|
ENSP00000503874.1:p.Lys213Thr
|
|
|
ENST00000678920.1:n.871A>C
|
|
|
|
ENST00000679019.1:n.1483A>C
|
|
|
|
ENST00000679117.1:c.*528A>C
|
ENSP00000503240.1:n.*528A>C
|
|
|
ENST00000679339.1:n.1554A>C
|
|
|
|
ENST00000326739.8:c.713A>C
|
ENSP00000321584.4:p.Lys238Thr
|
|
|
ENST00000429182.5:c.507A>C
|
|
|
|
ENST00000442157.1:c.638A>C
|
ENSP00000403502.1:p.Lys213Thr
|
|
|
ENST00000462980.1:n.615A>C
|
|
|
|
ENST00000491610.1:n.673A>C
|
|
|
|
NM_000884.2:c.713A>C
|
NP_000875.2:p.Lys238Thr
|
|
|
XM_006713128.2:c.923A>C
|
XP_006713191.1:p.Lys308Thr
|
|
|
XM_006713128.3:c.923A>C
|
XP_006713191.1:p.Lys308Thr
|
|
|
XM_017006349.1:c.848A>C
|
XP_016861838.1:p.Lys283Thr
|
|
|
XM_017006350.1:c.848A>C
|
XP_016861839.1:p.Lys283Thr
|
|
|
NM_000884.3:c.713A>C
MANE Select
|
NP_000875.2:p.Lys238Thr
|
|
