ENST00000526189.3:c.576G>T
|
ENSP00000488104.2:p.Leu192=
|
|
ENST00000533357.5:c.657G>T
MANE Select
|
ENSP00000432943.1:p.Leu219=
|
|
ENST00000672287.2:c.69G>T
|
ENSP00000499818.2:p.Leu23=
|
|
ENST00000672602.2:c.657G>T
|
ENSP00000500814.2:p.Leu219=
|
|
ENST00000674861.1:n.720G>T
|
|
|
ENST00000463290.5:c.657G>T
|
ENSP00000431538.1:p.Leu219=
|
|
ENST00000476410.1:n.247G>T
|
|
|
ENST00000488271.1:n.95G>T
|
|
|
ENST00000491222.5:c.69G>T
|
ENSP00000431441.1:p.Leu23=
|
|
ENST00000526189.2:c.320G>T
|
|
|
ENST00000533357.4:c.657G>T
|
ENSP00000432943.1:p.Leu219=
|
|
NM_000530.6:c.657G>T , LRG_256t1:c.657G>T
|
NP_000521.2:p.Leu219=
|
|
NM_000530.7:c.657G>T
|
NP_000521.2:p.Leu219=
|
|
NM_001315491.1:c.657G>T
|
NP_001302420.1:p.Leu219=
|
|
XM_017001321.2:c.675+142G>T
|
XP_016856810.1:n.675+142G>T
|
|
NM_000530.8:c.657G>T
MANE Select
|
NP_000521.2:p.Leu219=
|
|
NM_001315491.2:c.657G>T
|
NP_001302420.1:p.Leu219=
|
|