ENST00000318158.11:c.598G=
MANE Select
|
ENSP00000313432.6:p.Val200=
|
|
ENST00000318158.10:c.598G=
|
ENSP00000313432.6:p.Val200=
|
|
ENST00000377824.8:n.635G=
|
|
|
ENST00000460882.5:n.625G=
|
|
|
ENST00000480596.5:n.1299G=
|
|
|
ENST00000482603.1:n.51G=
|
|
|
ENST00000491488.5:n.303G=
|
|
|
ENST00000494290.1:c.169G=
|
ENSP00000432021.1:p.Val57=
|
|
ENST00000497693.1:n.2131G=
|
|
|
ENST00000607784.1:c.598G=
|
ENSP00000475569.1:p.Val200=
|
|
NM_012203.1:c.598G=
|
NP_036335.1:p.Val200=
|
|
XM_005251631.1:c.277G=
|
XP_005251688.1:p.Val93=
|
|
XM_011518073.1:c.196G=
|
XP_011516375.1:p.Val66=
|
|
XR_929374.1:n.1043G=
|
|
|
XM_017015320.2:c.598G=
|
XP_016870809.1:p.Val200=
|
|
XM_017015321.2:c.598G=
|
XP_016870810.1:p.Val200=
|
|
XM_017015323.2:c.196G=
|
XP_016870812.1:p.Val66=
|
|
XM_024447716.1:c.871G=
|
XP_024303484.1:p.Val291=
|
|
XM_024447717.1:c.871G=
|
XP_024303485.1:p.Val291=
|
|
XR_002956828.1:n.886G=
|
|
|
XR_002956829.1:n.886G=
|
|
|
XR_002956830.1:n.657G=
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|
XR_002956831.1:n.332G=
|
|
|
XR_002956832.1:n.1017G=
|
|
|
NM_012203.2:c.598G=
MANE Select
|
NP_036335.1:p.Val200=
|
|