ENST00000389857.11:c.5163G=
MANE Select
|
ENSP00000374507.6:p.Gly1721=
|
|
ENST00000331194.8:c.735G=
|
ENSP00000330332.8:p.Gly245=
|
|
ENST00000334448.5:n.975G=
|
|
|
ENST00000389857.10:c.5163G=
|
ENSP00000374507.6:p.Gly1721=
|
|
ENST00000556726.5:c.1391G=
|
|
|
NM_001080414.3:c.5163G=
|
NP_001073883.2:p.Gly1721=
|
|
XM_011536796.1:c.5055G=
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XP_011535098.1:p.Gly1685=
|
|
XR_429316.2:n.5438G=
|
|
|
XM_011536796.2:c.5055G=
|
XP_011535098.1:p.Gly1685=
|
|
XM_017021336.1:c.2244G=
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XP_016876825.1:p.Gly748=
|
|
XR_429316.4:n.5436G=
|
|
|
NM_001080414.4:c.5163G=
MANE Select
|
NP_001073883.2:p.Gly1721=
|
|