ENST00000371820.4:c.5158G>T
|
ENSP00000360885.4:p.Gly1720Cys
|
|
ENST00000371817.8:c.5158G>T
MANE Select
|
ENSP00000360882.3:p.Gly1720Cys
|
|
ENST00000371817.7:c.5158G>T
|
ENSP00000360882.3:p.Gly1720Cys
|
|
ENST00000371820.3:c.416G>T
|
|
|
ENST00000618395.4:c.5158G>T
|
ENSP00000481360.1:p.Gly1720Cys
|
|
NM_000093.4:c.5158G>T
|
NP_000084.3:p.Gly1720Cys
|
|
NM_001278074.1:c.5158G>T
|
NP_001265003.1:p.Gly1720Cys
|
|
NR_103451.2:n.71-14783C>A
|
|
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XR_929712.1:n.5842G>T
|
|
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XR_929713.1:n.5710G>T
|
|
|
NM_000093.5:c.5158G>T
MANE Select
|
NP_000084.3:p.Gly1720Cys
|
|