ENST00000399668.7:c.6286A>G
MANE Select
|
ENSP00000382576.3:p.Arg2096Gly
|
|
ENST00000346991.9:c.6364A>G
|
ENSP00000335463.6:p.Arg2122Gly
|
|
ENST00000399668.6:c.6286A>G
|
ENSP00000382576.2:p.Arg2096Gly
|
|
ENST00000526913.5:c.3419A>G
|
|
|
ENST00000532347.1:n.366A>G
|
|
|
NM_144508.4:c.6286A>G
|
NP_653091.3:p.Arg2096Gly
|
|
NM_170589.4:c.6364A>G
|
NP_733468.3:p.Arg2122Gly
|
|
XM_011521816.1:c.5962A>G
|
XP_011520118.1:p.Arg1988Gly
|
|
XM_011521817.1:c.6286A>G
|
XP_011520119.1:p.Arg2096Gly
|
|
XM_017022432.1:c.5962A>G
|
XP_016877921.1:p.Arg1988Gly
|
|
NM_144508.5:c.6286A>G
MANE Select
|
NP_653091.3:p.Arg2096Gly
|
|
NM_170589.5:c.6364A>G
|
NP_733468.3:p.Arg2122Gly
|
|