ENST00000282541.10:c.126C>G
MANE Select
|
ENSP00000282541.6:p.Val42=
|
|
ENST00000282541.9:c.126C>G
|
ENSP00000282541.5:p.Val42=
|
|
ENST00000425459.5:c.126C>G
|
ENSP00000408770.1:p.Val42=
|
|
ENST00000428684.1:c.48-10433C>G
|
ENSP00000392199.1:n.48-10433C>G
|
|
ENST00000429432.5:c.9C>G
|
ENSP00000393861.1:p.Val3=
|
|
ENST00000431009.1:c.9C>G
|
ENSP00000416518.1:p.Val3=
|
|
NM_015141.3:c.126C>G , LRG_419t1:c.126C>G
|
NP_055956.1:p.Val42=
|
|
XM_005264983.2:c.126C>G
|
XP_005265040.1:p.Val42=
|
|
XM_006713068.2:c.126C>G
|
XP_006713131.1:p.Val42=
|
|
NM_015141.4:c.126C>G
MANE Select
|
NP_055956.1:p.Val42=
|
|