ENST00000318158.11:c.751C>G
MANE Select
|
ENSP00000313432.6:p.Gln251Glu
|
|
ENST00000318158.10:c.751C>G
|
ENSP00000313432.6:p.Gln251Glu
|
|
ENST00000460882.5:n.778C>G
|
|
|
ENST00000480596.5:n.1452C>G
|
|
|
ENST00000482603.1:n.204C>G
|
|
|
ENST00000491488.5:n.456C>G
|
|
|
ENST00000494290.1:c.*51+873C>G
|
ENSP00000432021.1:n.*51+873C>G
|
|
ENST00000497693.1:n.4319C>G
|
|
|
ENST00000607784.1:c.751C>G
|
ENSP00000475569.1:p.Gln251Glu
|
|
NM_012203.1:c.751C>G
|
NP_036335.1:p.Gln251Glu
|
|
XM_005251631.1:c.430C>G
|
XP_005251688.1:p.Gln144Glu
|
|
XM_011518073.1:c.349C>G
|
XP_011516375.1:p.Gln117Glu
|
|
XM_017015320.2:c.751C>G
|
XP_016870809.1:p.Gln251Glu
|
|
XM_017015321.2:c.751C>G
|
XP_016870810.1:p.Gln251Glu
|
|
XM_017015323.2:c.349C>G
|
XP_016870812.1:p.Gln117Glu
|
|
XM_024447716.1:c.1024C>G
|
XP_024303484.1:p.Gln342Glu
|
|
XM_024447717.1:c.1024C>G
|
XP_024303485.1:p.Gln342Glu
|
|
XR_002956828.1:n.1039C>G
|
|
|
XR_002956829.1:n.1039C>G
|
|
|
XR_002956830.1:n.2171C>G
|
|
|
XR_002956831.1:n.1846C>G
|
|
|
XR_002956832.1:n.1170C>G
|
|
|
NM_012203.2:c.751C>G
MANE Select
|
NP_036335.1:p.Gln251Glu
|
|