|
ENST00000367698.4:c.1279C>T
MANE Select
|
ENSP00000356671.3:p.Leu427=
|
|
|
ENST00000367698.3:c.1279C>T
|
ENSP00000356671.3:p.Leu427=
|
|
|
ENST00000617423.4:c.664C>T
|
ENSP00000478688.1:p.Leu222=
|
|
|
NM_000488.3:c.1279C>T , LRG_577t1:c.1279C>T
|
NP_000479.1:p.Leu427=
|
|
|
XM_005245198.2:c.1135C>T
|
XP_005245255.1:p.Leu379=
|
|
|
NM_001365052.1:c.1135C>T
|
NP_001351981.1:p.Leu379=
|
|
|
NM_000488.4:c.1279C>T
MANE Select
|
NP_000479.1:p.Leu427=
|
|
|
NM_001365052.2:c.1135C>T
|
NP_001351981.1:p.Leu379=
|
|
|
NM_001386302.1:c.1402C>T
|
NP_001373231.1:p.Leu468=
|
|
|
NM_001386303.1:c.1360C>T
|
NP_001373232.1:p.Leu454=
|
|
|
NM_001386304.1:c.1258C>T
|
NP_001373233.1:p.Leu420=
|
|
|
NM_001386305.1:c.1222C>T
|
NP_001373234.1:p.Leu408=
|
|
|
NM_001386306.1:c.1063C>T
|
NP_001373235.1:p.Leu355=
|
|
