ENST00000261609.13:c.11809A>G
MANE Select
|
ENSP00000261609.8:p.Met3937Val
|
|
ENST00000650509.1:c.3520A>G
|
ENSP00000496936.1:p.Met1174Val
|
|
ENST00000261609.11:c.11809A>G
|
ENSP00000261609.7:p.Met3937Val
|
|
NM_004667.5:c.11809A>G
|
NP_004658.3:p.Met3937Val
|
|
XM_005268276.3:c.11695A>G
|
XP_005268333.1:p.Met3899Val
|
|
XM_005268277.3:c.11695A>G
|
XP_005268334.1:p.Met3899Val
|
|
XM_006720726.2:c.11794A>G
|
XP_006720789.1:p.Met3932Val
|
|
XM_006720727.2:c.11551A>G
|
XP_006720790.1:p.Met3851Val
|
|
XM_011522131.1:c.11326A>G
|
XP_011520433.1:p.Met3776Val
|
|
XM_011522132.1:c.9325A>G
|
XP_011520434.1:p.Met3109Val
|
|
XM_011522133.1:c.8554A>G
|
XP_011520435.1:p.Met2852Val
|
|
XM_011522134.1:c.5926A>G
|
XP_011520436.1:p.Met1976Val
|
|
XM_005268276.5:c.11695A>G
|
XP_005268333.1:p.Met3899Val
|
|
XM_006720726.3:c.11794A>G
|
XP_006720789.1:p.Met3932Val
|
|
XM_006720727.3:c.11551A>G
|
XP_006720790.1:p.Met3851Val
|
|
XM_017022695.1:c.11695A>G
|
XP_016878184.1:p.Met3899Val
|
|
XM_017022696.1:c.11695A>G
|
XP_016878185.1:p.Met3899Val
|
|
XM_017022697.1:c.4975A>G
|
XP_016878186.1:p.Met1659Val
|
|
XM_017022698.1:c.4975A>G
|
XP_016878187.1:p.Met1659Val
|
|
NM_004667.6:c.11809A>G
MANE Select
|
NP_004658.3:p.Met3937Val
|
|