ENST00000696142.1:c.*271G>C
|
ENSP00000512434.1:n.*271G>C
|
|
ENST00000696143.1:c.730G>C
|
ENSP00000512435.1:n.730G>C
|
|
ENST00000696153.1:c.705G>C
|
ENSP00000512444.1:p.Leu235=
|
|
ENST00000256474.3:c.594G>C
MANE Select
|
ENSP00000256474.3:p.Leu198=
|
|
ENST00000256474.2:c.594G>C
|
ENSP00000256474.2:p.Leu198=
|
|
ENST00000345392.2:c.471G>C
|
ENSP00000344757.2:p.Leu157=
|
|
ENST00000477538.1:n.730G>C
|
|
|
NM_000551.3:c.594G>C , LRG_322t1:c.594G>C
|
NP_000542.1:p.Leu198=
|
|
NM_198156.2:c.471G>C
|
NP_937799.1:p.Leu157=
|
|
NM_001354723.1:c.*148G>C
|
NP_001341652.1:n.*148G>C
|
|
NM_000551.4:c.594G>C
MANE Select
|
NP_000542.1:p.Leu198=
|
|
NM_001354723.2:c.*148G>C
|
NP_001341652.1:n.*148G>C
|
|
NM_198156.3:c.471G>C
|
NP_937799.1:p.Leu157=
|
|