ENST00000318158.11:c.549A>T
MANE Select
|
ENSP00000313432.6:p.Thr183=
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|
ENST00000318158.10:c.549A>T
|
ENSP00000313432.6:p.Thr183=
|
|
ENST00000377824.8:n.586A>T
|
|
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ENST00000460882.5:n.576A>T
|
|
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ENST00000480596.5:n.1250A>T
|
|
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ENST00000482603.1:n.2A>T
|
|
|
ENST00000491488.5:n.254A>T
|
|
|
ENST00000494290.1:c.120A>T
|
ENSP00000432021.1:p.Thr40=
|
|
ENST00000497693.1:n.2082A>T
|
|
|
ENST00000607784.1:c.549A>T
|
ENSP00000475569.1:p.Thr183=
|
|
NM_012203.1:c.549A>T
|
NP_036335.1:p.Thr183=
|
|
XM_005251631.1:c.228A>T
|
XP_005251688.1:p.Thr76=
|
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XM_011518073.1:c.147A>T
|
XP_011516375.1:p.Thr49=
|
|
XR_929374.1:n.994A>T
|
|
|
XM_017015320.2:c.549A>T
|
XP_016870809.1:p.Thr183=
|
|
XM_017015321.2:c.549A>T
|
XP_016870810.1:p.Thr183=
|
|
XM_017015323.2:c.147A>T
|
XP_016870812.1:p.Thr49=
|
|
XM_024447716.1:c.822A>T
|
XP_024303484.1:p.Thr274=
|
|
XM_024447717.1:c.822A>T
|
XP_024303485.1:p.Thr274=
|
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XR_002956828.1:n.837A>T
|
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XR_002956829.1:n.837A>T
|
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XR_002956830.1:n.608A>T
|
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XR_002956831.1:n.283A>T
|
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XR_002956832.1:n.968A>T
|
|
|
NM_012203.2:c.549A>T
MANE Select
|
NP_036335.1:p.Thr183=
|
|