|
ENST00000367698.4:c.922G>C
MANE Select
|
ENSP00000356671.3:p.Gly308Arg
|
|
|
ENST00000367698.3:c.922G>C
|
ENSP00000356671.3:p.Gly308Arg
|
|
|
ENST00000487183.1:n.573G>C
|
|
|
|
ENST00000617423.4:c.559+2081G>C
|
ENSP00000478688.1:n.559+2081G>C
|
|
|
NM_000488.3:c.922G>C , LRG_577t1:c.922G>C
|
NP_000479.1:p.Gly308Arg
|
|
|
XM_005245198.2:c.778G>C
|
XP_005245255.1:p.Gly260Arg
|
|
|
NM_001365052.1:c.778G>C
|
NP_001351981.1:p.Gly260Arg
|
|
|
NM_000488.4:c.922G>C
MANE Select
|
NP_000479.1:p.Gly308Arg
|
|
|
NM_001365052.2:c.778G>C
|
NP_001351981.1:p.Gly260Arg
|
|
|
NM_001386302.1:c.1045G>C
|
NP_001373231.1:p.Gly349Arg
|
|
|
NM_001386303.1:c.1003G>C
|
NP_001373232.1:p.Gly335Arg
|
|
|
NM_001386304.1:c.901G>C
|
NP_001373233.1:p.Gly301Arg
|
|
|
NM_001386305.1:c.865G>C
|
NP_001373234.1:p.Gly289Arg
|
|
|
NM_001386306.1:c.706G>C
|
NP_001373235.1:p.Gly236Arg
|
|
