ENST00000557915.2:n.1512G>T
|
|
|
ENST00000557921.3:c.*144G>T
|
ENSP00000453157.3:n.*144G>T
|
|
ENST00000699682.1:n.1599G>T
|
|
|
ENST00000699683.1:n.1649G>T
|
|
|
ENST00000699684.1:c.*802G>T
|
ENSP00000514523.1:n.*802G>T
|
|
ENST00000699685.1:n.1413G>T
|
|
|
ENST00000699686.1:c.*144G>T
|
ENSP00000514524.1:n.*144G>T
|
|
ENST00000699687.1:c.*144G>T
|
ENSP00000514525.1:n.*144G>T
|
|
ENST00000699688.1:n.1409G>T
|
|
|
ENST00000699689.1:n.1765G>T
|
|
|
ENST00000699690.1:n.1962G>T
|
|
|
ENST00000699691.1:n.2106G>T
|
|
|
ENST00000699692.1:n.60G>T
|
|
|
ENST00000699693.1:n.1538G>T
|
|
|
ENST00000699694.1:n.1868G>T
|
|
|
ENST00000699695.1:c.*493G>T
|
ENSP00000514526.1:n.*493G>T
|
|
ENST00000699696.1:n.1512G>T
|
|
|
ENST00000699697.1:c.1121G>T
|
ENSP00000514527.1:p.Arg374Met
|
|
ENST00000699698.1:n.1042G>T
|
|
|
ENST00000699699.1:n.1533G>T
|
|
|
ENST00000699700.1:n.1656G>T
|
|
|
ENST00000699701.1:c.*589G>T
|
ENSP00000514528.1:n.*589G>T
|
|
ENST00000267415.12:c.1121G>T
MANE Select
|
ENSP00000267415.7:p.Arg374Met
|
|
ENST00000646753.1:c.1016G>T
|
ENSP00000494065.1:p.Arg339Met
|
|
ENST00000267415.11:c.1121G>T
|
ENSP00000267415.7:p.Arg374Met
|
|
ENST00000399423.8:c.*144G>T
|
ENSP00000382350.4:n.*144G>T
|
|
ENST00000557915.1:n.328G>T
|
|
|
ENST00000558566.1:c.*581G>T
|
ENSP00000453025.1:n.*581G>T
|
|
ENST00000559969.5:c.967G>T
|
|
|
ENST00000560019.5:c.116G>T
|
ENSP00000453113.1:p.Arg39Met
|
|
ENST00000626689.2:c.*493G>T
|
ENSP00000486681.1:n.*493G>T
|
|
NM_001099274.1:c.1121G>T
|
NP_001092744.1:p.Arg374Met
|
|
NM_012461.2:c.*144G>T
|
NP_036593.2:n.*144G>T
|
|
XM_005267528.2:c.1121G>T
|
XP_005267585.1:p.Arg374Met
|
|
XM_005267529.2:c.1016G>T
|
XP_005267586.1:p.Arg339Met
|
|
NM_001099274.2:c.1121G>T
|
NP_001092744.1:p.Arg374Met
|
|
NM_001363668.1:c.1016G>T
|
NP_001350597.1:p.Arg339Met
|
|
NM_012461.3:c.*144G>T
|
NP_036593.2:n.*144G>T
|
|
XM_011536642.2:c.*589G>T
|
XP_011534944.1:n.*589G>T
|
|
XM_017021216.2:c.479G>T
|
XP_016876705.1:p.Arg160Met
|
|
XM_017021217.1:c.479G>T
|
XP_016876706.1:p.Arg160Met
|
|
NM_001099274.3:c.1121G>T
MANE Select
|
NP_001092744.1:p.Arg374Met
|
|
NM_001363668.2:c.1016G>T
|
NP_001350597.1:p.Arg339Met
|
|