ENST00000264595.7:c.555T>A
MANE Select
|
ENSP00000264595.2:p.Pro185=
|
|
ENST00000264595.6:c.555T>A
|
ENSP00000264595.2:p.Pro185=
|
|
ENST00000502310.5:c.210T>A
|
ENSP00000423798.1:p.Pro70=
|
|
ENST00000506853.5:n.589T>A
|
|
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ENST00000510635.1:c.251T>A
|
|
|
ENST00000510955.5:n.476T>A
|
|
|
NM_000027.3:c.555T>A
|
NP_000018.2:p.Pro185=
|
|
NM_001171988.1:c.555T>A
|
NP_001165459.1:p.Pro185=
|
|
NR_033655.1:n.683T>A
|
|
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XM_006714123.2:c.555T>A
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XP_006714186.1:p.Pro185=
|
|
XR_001741155.2:n.649T>A
|
|
|
NM_000027.4:c.555T>A
MANE Select
|
NP_000018.2:p.Pro185=
|
|
NM_001171988.2:c.555T>A
|
NP_001165459.1:p.Pro185=
|
|
NR_033655.2:n.617T>A
|
|
|