ENST00000557915.2:n.1115A=
|
|
|
ENST00000557921.3:c.704A=
|
ENSP00000453157.3:p.Gln235=
|
|
ENST00000699682.1:n.1202A=
|
|
|
ENST00000699683.1:n.1252A=
|
|
|
ENST00000699684.1:c.*405A=
|
ENSP00000514523.1:n.*405A=
|
|
ENST00000699685.1:n.1016A=
|
|
|
ENST00000699686.1:c.605A=
|
ENSP00000514524.1:p.Gln202=
|
|
ENST00000699687.1:c.707A=
|
ENSP00000514525.1:p.Gln236=
|
|
ENST00000699688.1:n.1012A=
|
|
|
ENST00000699689.1:n.1368A=
|
|
|
ENST00000699690.1:n.1565A=
|
|
|
ENST00000699691.1:n.1709A=
|
|
|
ENST00000699693.1:n.1229A=
|
|
|
ENST00000699694.1:n.1471A=
|
|
|
ENST00000699695.1:c.*184A=
|
ENSP00000514526.1:n.*184A=
|
|
ENST00000699696.1:n.1115A=
|
|
|
ENST00000699697.1:c.812A=
|
ENSP00000514527.1:p.Gln271=
|
|
ENST00000699698.1:n.733A=
|
|
|
ENST00000699699.1:n.1136A=
|
|
|
ENST00000699700.1:n.1259A=
|
|
|
ENST00000699701.1:c.*192A=
|
ENSP00000514528.1:n.*192A=
|
|
ENST00000267415.12:c.812A=
MANE Select
|
ENSP00000267415.7:p.Gln271=
|
|
ENST00000557921.2:c.704A=
|
ENSP00000453157.2:p.Gln235=
|
|
ENST00000646753.1:c.707A=
|
ENSP00000494065.1:p.Gln236=
|
|
ENST00000267415.11:c.812A=
|
ENSP00000267415.7:p.Gln271=
|
|
ENST00000399423.8:c.812A=
|
ENSP00000382350.4:p.Gln271=
|
|
ENST00000558476.5:c.374A=
|
ENSP00000452724.1:p.Gln125=
|
|
ENST00000558566.1:c.*184A=
|
ENSP00000453025.1:n.*184A=
|
|
ENST00000559019.1:c.*184A=
|
ENSP00000453675.1:n.*184A=
|
|
ENST00000559549.1:n.538A=
|
|
|
ENST00000559969.5:c.757+11A=
|
|
|
ENST00000626689.2:c.*184A=
|
ENSP00000486681.1:n.*184A=
|
|
NM_001099274.1:c.812A=
|
NP_001092744.1:p.Gln271=
|
|
NM_012461.2:c.812A=
|
NP_036593.2:p.Gln271=
|
|
XM_005267528.2:c.812A=
|
XP_005267585.1:p.Gln271=
|
|
XM_005267529.2:c.707A=
|
XP_005267586.1:p.Gln236=
|
|
NM_001099274.2:c.812A=
|
NP_001092744.1:p.Gln271=
|
|
NM_001363668.1:c.707A=
|
NP_001350597.1:p.Gln236=
|
|
NM_012461.3:c.812A=
|
NP_036593.2:p.Gln271=
|
|
XM_011536642.2:c.*192A=
|
XP_011534944.1:n.*192A=
|
|
XM_017021216.2:c.170A=
|
XP_016876705.1:p.Gln57=
|
|
XM_017021217.1:c.170A=
|
XP_016876706.1:p.Gln57=
|
|
NM_001099274.3:c.812A=
MANE Select
|
NP_001092744.1:p.Gln271=
|
|
NM_001363668.2:c.707A=
|
NP_001350597.1:p.Gln236=
|
|