ENST00000333213.11:c.751A>G
MANE Select
|
ENSP00000327487.6:p.Met251Val
|
|
ENST00000434205.8:c.448A>G
|
ENSP00000406559.4:p.Met150Val
|
|
ENST00000545228.3:c.751A>G
|
ENSP00000438169.3:p.Met251Val
|
|
ENST00000579449.2:n.550A>G
|
|
|
ENST00000580013.6:n.954A>G
|
|
|
ENST00000583818.2:c.805A>G
|
ENSP00000461928.2:n.805A>G
|
|
ENST00000679370.1:n.1332A>G
|
|
|
ENST00000679429.1:c.*209A>G
|
ENSP00000505403.1:n.*209A>G
|
|
ENST00000679443.1:n.820A>G
|
|
|
ENST00000679782.1:c.751A>G
|
ENSP00000505995.1:p.Met251Val
|
|
ENST00000679919.1:n.820A>G
|
|
|
ENST00000679928.1:c.*362A>G
|
ENSP00000506071.1:n.*362A>G
|
|
ENST00000680528.1:n.776A>G
|
|
|
ENST00000680999.1:c.751A>G
|
ENSP00000504984.1:p.Met251Val
|
|
ENST00000681282.1:c.780A>G
|
ENSP00000506339.1:p.Pro260=
|
|
ENST00000333213.10:c.751A>G
|
ENSP00000327487.6:p.Met251Val
|
|
ENST00000578415.1:c.711A>G
|
|
|
ENST00000583173.5:c.459-175A>G
|
ENSP00000463619.1:n.459-175A>G
|
|
ENST00000583818.1:c.700A>G
|
ENSP00000461928.1:n.700A>G
|
|
NM_207346.2:c.751A>G
|
NP_997229.2:p.Met251Val
|
|
XM_005257229.2:c.751A>G
|
XP_005257286.1:p.Met251Val
|
|
XM_006721821.2:c.448A>G
|
XP_006721884.1:p.Met150Val
|
|
XM_011524616.1:c.751A>G
|
XP_011522918.1:p.Met251Val
|
|
XM_011524617.1:c.751A>G
|
XP_011522919.1:p.Met251Val
|
|
XM_011524618.1:c.751A>G
|
XP_011522920.1:p.Met251Val
|
|
XR_243646.2:n.781A>G
|
|
|
XM_005257229.4:c.751A>G
|
XP_005257286.1:p.Met251Val
|
|
XR_243646.4:n.787A>G
|
|
|
NM_207346.3:c.751A>G
MANE Select
|
NP_997229.2:p.Met251Val
|
|