ENST00000367698.4:c.910T>C
MANE Select
|
ENSP00000356671.3:p.Leu304=
|
|
ENST00000367698.3:c.910T>C
|
ENSP00000356671.3:p.Leu304=
|
|
ENST00000487183.1:n.561T>C
|
|
|
ENST00000617423.4:c.559+2069T>C
|
ENSP00000478688.1:n.559+2069T>C
|
|
NM_000488.3:c.910T>C , LRG_577t1:c.910T>C
|
NP_000479.1:p.Leu304=
|
|
XM_005245198.2:c.766T>C
|
XP_005245255.1:p.Leu256=
|
|
NM_001365052.1:c.766T>C
|
NP_001351981.1:p.Leu256=
|
|
NM_000488.4:c.910T>C
MANE Select
|
NP_000479.1:p.Leu304=
|
|
NM_001365052.2:c.766T>C
|
NP_001351981.1:p.Leu256=
|
|
NM_001386302.1:c.1033T>C
|
NP_001373231.1:p.Leu345=
|
|
NM_001386303.1:c.991T>C
|
NP_001373232.1:p.Leu331=
|
|
NM_001386304.1:c.889T>C
|
NP_001373233.1:p.Leu297=
|
|
NM_001386305.1:c.853T>C
|
NP_001373234.1:p.Leu285=
|
|
NM_001386306.1:c.694T>C
|
NP_001373235.1:p.Leu232=
|
|