ENST00000318158.11:c.141A>T
MANE Select
|
ENSP00000313432.6:p.Arg47=
|
|
ENST00000318158.10:c.141A>T
|
ENSP00000313432.6:p.Arg47=
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|
ENST00000377824.8:n.178A>T
|
|
|
ENST00000460882.5:n.168A>T
|
|
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ENST00000487399.5:n.150A>T
|
|
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ENST00000491488.5:n.109+2069A>T
|
|
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ENST00000493368.5:n.198A>T
|
|
|
ENST00000607784.1:c.141A>T
|
ENSP00000475569.1:p.Arg47=
|
|
NM_012203.1:c.141A>T
|
NP_036335.1:p.Arg47=
|
|
XM_005251631.1:c.83+2069A>T
|
XP_005251688.1:n.83+2069A>T
|
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XM_011518073.1:c.-622A>T
|
XP_011516375.1:n.-622A>T
|
|
XR_929374.1:n.226A>T
|
|
|
XM_017015320.2:c.141A>T
|
XP_016870809.1:p.Arg47=
|
|
XM_017015321.2:c.141A>T
|
XP_016870810.1:p.Arg47=
|
|
XM_017015323.2:c.-622A>T
|
XP_016870812.1:n.-622A>T
|
|
XM_024447716.1:c.414A>T
|
XP_024303484.1:p.Arg138=
|
|
XM_024447717.1:c.414A>T
|
XP_024303485.1:p.Arg138=
|
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XR_002956828.1:n.429A>T
|
|
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XR_002956829.1:n.429A>T
|
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XR_002956830.1:n.200A>T
|
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|
XR_002956831.1:n.138+2069A>T
|
|
|
XR_002956832.1:n.200A>T
|
|
|
NM_012203.2:c.141A>T
MANE Select
|
NP_036335.1:p.Arg47=
|
|