|
NM_015141.4:c.1A>G
MANE Select
|
NP_055956.1:p.Met1Val
|
|
ENST00000282541.10:c.1A>G
MANE Select
|
ENSP00000282541.6:p.Met1Val
|
|
NM_015141.3:c.1A>G , LRG_419t1:c.1A>G
|
NP_055956.1:p.Met1Val
|
|
ENST00000282541.9:c.1A>G
|
ENSP00000282541.5:p.Met1Val
|
|
ENST00000425459.5:c.1A>G
|
ENSP00000408770.1:p.Met1Val
|
|
ENST00000428684.1:c.1A>G
|
ENSP00000392199.1:p.Met1Val
|
|
ENST00000429432.5:c.-71+883A>G
|
ENSP00000393861.1:n.-71+883A>G
|
|
ENST00000431009.1:c.-176A>G
|
ENSP00000416518.1:n.-176A>G
|
|
XM_005264983.2:c.1A>G
|
XP_005265040.1:p.Met1Val
|
|
XM_006713068.2:c.1A>G
|
XP_006713131.1:p.Met1Val
|