ENST00000389857.11:c.5059-129T>C
MANE Select
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ENSP00000374507.6:n.5059-129T>C
|
|
ENST00000331194.8:c.631-129T>C
|
ENSP00000330332.8:n.631-129T>C
|
|
ENST00000334448.5:n.871-129T>C
|
|
|
ENST00000389857.10:c.5059-129T>C
|
ENSP00000374507.6:n.5059-129T>C
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|
ENST00000556726.5:c.1287-129T>C
|
|
|
NM_001080414.3:c.5059-129T>C
|
NP_001073883.2:n.5059-129T>C
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|
XM_011536796.1:c.4951-129T>C
|
XP_011535098.1:n.4951-129T>C
|
|
XR_429316.2:n.5334-129T>C
|
|
|
XM_011536796.2:c.4951-129T>C
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XP_011535098.1:n.4951-129T>C
|
|
XM_017021336.1:c.2140-129T>C
|
XP_016876825.1:n.2140-129T>C
|
|
XR_429316.4:n.5332-129T>C
|
|
|
NM_001080414.4:c.5059-129T>C
MANE Select
|
NP_001073883.2:n.5059-129T>C
|
|