|
NM_012203.2:c.667G>A
MANE Select
|
NP_036335.1:p.Glu223Lys
|
|
ENST00000318158.11:c.667G>A
MANE Select
|
ENSP00000313432.6:p.Glu223Lys
|
|
NM_012203.1:c.667G>A
|
NP_036335.1:p.Glu223Lys
|
|
ENST00000318158.10:c.667G>A
|
ENSP00000313432.6:p.Glu223Lys
|
|
ENST00000377824.8:n.704G>A
|
|
|
ENST00000460882.5:n.694G>A
|
|
|
ENST00000480596.5:n.1368G>A
|
|
|
ENST00000482603.1:n.120G>A
|
|
|
ENST00000491488.5:n.372G>A
|
|
|
ENST00000494290.1:c.238G>A
|
ENSP00000432021.1:p.Glu80Lys
|
|
ENST00000497693.1:n.2874G>A
|
|
|
ENST00000607784.1:c.667G>A
|
ENSP00000475569.1:p.Glu223Lys
|
|
XM_005251631.1:c.346G>A
|
XP_005251688.1:p.Glu116Lys
|
|
XM_011518073.1:c.265G>A
|
XP_011516375.1:p.Glu89Lys
|
|
XM_017015320.2:c.667G>A
|
XP_016870809.1:p.Glu223Lys
|
|
XM_017015321.2:c.667G>A
|
XP_016870810.1:p.Glu223Lys
|
|
XM_017015323.2:c.265G>A
|
XP_016870812.1:p.Glu89Lys
|
|
XM_024447716.1:c.940G>A
|
XP_024303484.1:p.Glu314Lys
|
|
XM_024447717.1:c.940G>A
|
XP_024303485.1:p.Glu314Lys
|
|
XR_002956828.1:n.955G>A
|
|
|
XR_002956829.1:n.955G>A
|
|
|
XR_002956830.1:n.726G>A
|
|
|
XR_002956831.1:n.401G>A
|
|
|
XR_002956832.1:n.1086G>A
|
|
|
XR_929374.1:n.1112G>A
|
|