ENST00000318158.11:c.543G>A
MANE Select
|
ENSP00000313432.6:p.Leu181=
|
|
ENST00000318158.10:c.543G>A
|
ENSP00000313432.6:p.Leu181=
|
|
ENST00000377824.8:n.580G>A
|
|
|
ENST00000460882.5:n.570G>A
|
|
|
ENST00000480596.5:n.1244G>A
|
|
|
ENST00000491488.5:n.248G>A
|
|
|
ENST00000494290.1:c.114G>A
|
ENSP00000432021.1:p.Leu38=
|
|
ENST00000497693.1:n.2076G>A
|
|
|
ENST00000607784.1:c.543G>A
|
ENSP00000475569.1:p.Leu181=
|
|
NM_012203.1:c.543G>A
|
NP_036335.1:p.Leu181=
|
|
XM_005251631.1:c.222G>A
|
XP_005251688.1:p.Leu74=
|
|
XM_011518073.1:c.141G>A
|
XP_011516375.1:p.Leu47=
|
|
XR_929374.1:n.988G>A
|
|
|
XM_017015320.2:c.543G>A
|
XP_016870809.1:p.Leu181=
|
|
XM_017015321.2:c.543G>A
|
XP_016870810.1:p.Leu181=
|
|
XM_017015323.2:c.141G>A
|
XP_016870812.1:p.Leu47=
|
|
XM_024447716.1:c.816G>A
|
XP_024303484.1:p.Leu272=
|
|
XM_024447717.1:c.816G>A
|
XP_024303485.1:p.Leu272=
|
|
XR_002956828.1:n.831G>A
|
|
|
XR_002956829.1:n.831G>A
|
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XR_002956830.1:n.602G>A
|
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|
XR_002956831.1:n.277G>A
|
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|
XR_002956832.1:n.962G>A
|
|
|
NM_012203.2:c.543G>A
MANE Select
|
NP_036335.1:p.Leu181=
|
|