ENST00000313601.11:c.471G>C
MANE Select
|
ENSP00000312999.6:p.Leu157=
|
|
ENST00000266027.9:c.315G>C
|
ENSP00000266027.6:p.Leu105=
|
|
ENST00000313601.10:c.471G>C
|
ENSP00000312999.6:p.Leu157=
|
|
ENST00000422163.5:c.423G>C
|
ENSP00000406871.1:p.Leu141=
|
|
ENST00000440628.5:c.315G>C
|
ENSP00000395736.1:p.Leu105=
|
|
ENST00000441156.5:c.428G>C
|
ENSP00000394321.1:p.Ter143Ser
|
|
ENST00000446079.5:c.*106G>C
|
ENSP00000406065.1:n.*106G>C
|
|
ENST00000451956.1:c.360G>C
|
ENSP00000406369.1:p.Leu120=
|
|
ENST00000468422.1:n.38G>C
|
|
|
ENST00000490122.5:n.1298G>C
|
|
|
ENST00000491100.5:n.2287G>C
|
|
|
NM_001166425.1:c.360G>C
|
NP_001159897.1:p.Leu120=
|
|
NM_001282617.1:c.315G>C
|
NP_001269546.1:p.Leu105=
|
|
NM_001282618.1:c.228G>C
|
NP_001269547.1:p.Leu76=
|
|
NM_001282619.1:c.423G>C
|
NP_001269548.1:p.Leu141=
|
|
NM_001282620.1:c.423G>C
|
NP_001269549.1:p.Leu141=
|
|
NM_002070.3:c.471G>C
|
NP_002061.1:p.Leu157=
|
|
NM_002070.4:c.471G>C
MANE Select
|
NP_002061.1:p.Leu157=
|
|
NM_001166425.2:c.360G>C
|
NP_001159897.1:p.Leu120=
|
|
NM_001282618.2:c.228G>C
|
NP_001269547.1:p.Leu76=
|
|
NM_001282619.2:c.423G>C
|
NP_001269548.1:p.Leu141=
|
|
NM_001282620.2:c.423G>C
|
NP_001269549.1:p.Leu141=
|
|
NM_001282617.2:c.315G>C
|
NP_001269546.1:p.Leu105=
|
|