ENST00000703936.1:c.2726A>T
|
ENSP00000515567.1:p.Lys909Met
|
|
ENST00000703937.1:c.*1787A>T
|
ENSP00000515568.1:n.*1787A>T
|
|
ENST00000326739.9:c.686A>T
MANE Select
|
ENSP00000321584.4:p.Lys229Met
|
|
ENST00000429182.6:c.686A>T
|
ENSP00000393525.2:p.Lys229Met
|
|
ENST00000442157.2:c.611A>T
|
ENSP00000403502.2:p.Lys204Met
|
|
ENST00000462980.2:n.1201A>T
|
|
|
ENST00000472328.2:n.752A>T
|
|
|
ENST00000491610.2:n.646A>T
|
|
|
ENST00000676607.1:n.982A>T
|
|
|
ENST00000676627.1:n.1416A>T
|
|
|
ENST00000676708.1:n.1966A>T
|
|
|
ENST00000676864.1:n.1835A>T
|
|
|
ENST00000677010.1:c.722A>T
|
ENSP00000503089.1:p.Lys241Met
|
|
ENST00000677108.1:n.2592A>T
|
|
|
ENST00000677168.1:n.1158A>T
|
|
|
ENST00000677185.1:n.1249A>T
|
|
|
ENST00000677205.1:n.1470A>T
|
|
|
ENST00000677344.1:n.1960A>T
|
|
|
ENST00000677480.1:c.*363A>T
|
ENSP00000504378.1:n.*363A>T
|
|
ENST00000677519.1:n.1396A>T
|
|
|
ENST00000677593.1:n.1242A>T
|
|
|
ENST00000677740.1:n.2191A>T
|
|
|
ENST00000677991.1:n.1859A>T
|
|
|
ENST00000678001.1:n.1179A>T
|
|
|
ENST00000678085.1:n.1242A>T
|
|
|
ENST00000678177.1:n.2535A>T
|
|
|
ENST00000678603.1:n.1764A>T
|
|
|
ENST00000678724.1:c.611A>T
|
ENSP00000503874.1:p.Lys204Met
|
|
ENST00000678920.1:n.844A>T
|
|
|
ENST00000679019.1:n.1456A>T
|
|
|
ENST00000679117.1:c.*501A>T
|
ENSP00000503240.1:n.*501A>T
|
|
ENST00000679339.1:n.1527A>T
|
|
|
ENST00000326739.8:c.686A>T
|
ENSP00000321584.4:p.Lys229Met
|
|
ENST00000429182.5:c.480A>T
|
|
|
ENST00000442157.1:c.611A>T
|
ENSP00000403502.1:p.Lys204Met
|
|
ENST00000462980.1:n.588A>T
|
|
|
ENST00000491610.1:n.646A>T
|
|
|
NM_000884.2:c.686A>T
|
NP_000875.2:p.Lys229Met
|
|
XM_006713128.2:c.896A>T
|
XP_006713191.1:p.Lys299Met
|
|
XM_006713128.3:c.896A>T
|
XP_006713191.1:p.Lys299Met
|
|
XM_017006349.1:c.821A>T
|
XP_016861838.1:p.Lys274Met
|
|
XM_017006350.1:c.821A>T
|
XP_016861839.1:p.Lys274Met
|
|
NM_000884.3:c.686A>T
MANE Select
|
NP_000875.2:p.Lys229Met
|
|