ENST00000261978.9:c.5420G>T
MANE Select
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ENSP00000261978.4:p.Gly1807Val
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ENST00000261978.8:c.5420G>T
|
ENSP00000261978.4:p.Gly1807Val
|
|
ENST00000553939.5:c.*199G>T
|
ENSP00000452110.1:n.*199G>T
|
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ENST00000554861.1:n.638G>T
|
|
|
ENST00000556690.5:c.5288G>T
|
ENSP00000451477.1:p.Gly1763Val
|
|
NM_000428.2:c.5420G>T
|
NP_000419.1:p.Gly1807Val
|
|
XM_011536765.1:c.5039G>T
|
XP_011535067.1:p.Gly1680Val
|
|
XM_011536766.1:c.4961G>T
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XP_011535068.1:p.Gly1654Val
|
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XM_011536767.1:c.4937G>T
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XP_011535069.1:p.Gly1646Val
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XM_011536765.2:c.5039G>T
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XP_011535067.1:p.Gly1680Val
|
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NM_000428.3:c.5420G>T
MANE Select
|
NP_000419.1:p.Gly1807Val
|
|