ENST00000310926.11:c.664G>C
MANE Select
|
ENSP00000311291.4:p.Gly222Arg
|
|
ENST00000310926.8:c.664G>C
|
ENSP00000311291.4:p.Gly222Arg
|
|
ENST00000462770.5:n.521-5023G>C
|
|
|
ENST00000464676.5:n.926G>C
|
|
|
ENST00000481359.3:c.664G>C
|
ENSP00000420028.3:p.Gly222Arg
|
|
ENST00000493729.5:c.436G>C
|
ENSP00000418893.1:p.Gly146Arg
|
|
NM_005630.2:c.664G>C
|
NP_005621.2:p.Gly222Arg
|
|
XM_011513090.1:c.664G>C
|
XP_011511392.1:p.Gly222Arg
|
|
XM_017007077.1:c.160G>C
|
XP_016862566.1:p.Gly54Arg
|
|
XM_024453721.1:c.664G>C
|
XP_024309489.1:p.Gly222Arg
|
|
NM_005630.3:c.664G>C
MANE Select
|
NP_005621.2:p.Gly222Arg
|
|