ENST00000366159.9:n.524A=
|
|
|
ENST00000437813.8:c.490A=
|
ENSP00000513672.1:p.Thr164=
|
|
ENST00000440083.7:c.709A=
|
ENSP00000413224.3:p.Thr237=
|
|
ENST00000535958.2:c.*317A=
|
ENSP00000513673.1:n.*317A=
|
|
ENST00000698339.1:c.490A=
|
ENSP00000513670.1:p.Thr164=
|
|
ENST00000698340.1:c.490A=
|
ENSP00000513671.1:p.Thr164=
|
|
ENST00000162749.7:c.490A=
MANE Select
|
ENSP00000162749.2:p.Thr164=
|
|
ENST00000162749.6:c.490A=
|
ENSP00000162749.2:p.Thr164=
|
|
ENST00000366159.8:c.490A=
|
ENSP00000380389.3:p.Thr164=
|
|
ENST00000437813.7:n.451A=
|
|
|
ENST00000440083.6:c.709A=
|
ENSP00000413224.2:p.Thr237=
|
|
ENST00000534885.5:c.336A=
|
ENSP00000441803.1:p.Thr112=
|
|
ENST00000537842.5:n.94A=
|
|
|
ENST00000539372.5:c.490A=
|
ENSP00000442059.1:p.Thr164=
|
|
ENST00000540022.5:c.361A=
|
ENSP00000438343.1:p.Thr121=
|
|
ENST00000543048.5:c.*101A=
|
ENSP00000439981.1:n.*101A=
|
|
ENST00000543995.5:c.*77A=
|
ENSP00000442405.1:n.*77A=
|
|
NM_001065.3:c.490A= , LRG_193t1:c.490A=
|
NP_001056.1:p.Thr164=
|
|
NM_001346091.1:c.166A=
|
NP_001333020.1:p.Thr56=
|
|
NM_001346092.1:c.-88A=
|
NP_001333021.1:n.-88A=
|
|
NR_144351.1:n.793A=
|
|
|
NM_001065.4:c.490A=
MANE Select
|
NP_001056.1:p.Thr164=
|
|
NM_001346091.2:c.166A=
|
NP_001333020.1:p.Thr56=
|
|
NM_001346092.2:c.-88A=
|
NP_001333021.1:n.-88A=
|
|
NR_144351.2:n.752A=
|
|
|