ENST00000392492.8:c.487G>T
MANE Select
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ENSP00000376282.2:p.Ala163Ser
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ENST00000250615.7:c.622G>T
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ENSP00000250615.2:p.Ala208Ser
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ENST00000392492.7:c.487G>T
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ENSP00000376282.2:p.Ala163Ser
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ENST00000587798.1:c.*264G>T
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ENSP00000468239.1:n.*264G>T
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NM_001088.2:c.487G>T
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NP_001079.1:p.Ala163Ser
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NM_001166579.1:c.622G>T
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NP_001160051.1:p.Ala208Ser
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NR_110548.1:n.798G>T
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XM_011524415.1:c.487G>T
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XP_011522717.1:p.Ala163Ser
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XM_011524416.1:c.694G>T
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XP_011522718.1:p.Ala232Ser
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XM_011524417.1:c.694G>T
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XP_011522719.1:p.Ala232Ser
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XM_011524418.1:c.694G>T
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XP_011522720.1:p.Ala232Ser
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XM_011524419.1:c.694G>T
|
XP_011522721.1:p.Ala232Ser
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XM_011524420.1:c.694G>T
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XP_011522722.1:p.Ala232Ser
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XM_011524421.1:c.694G>T
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XP_011522723.1:p.Ala232Ser
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XM_011524422.1:c.577G>T
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XP_011522724.1:p.Ala193Ser
|
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XM_011524423.1:c.487G>T
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XP_011522725.1:p.Ala163Ser
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XM_017024259.1:c.601G>T
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XP_016879748.1:p.Ala201Ser
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NM_001088.3:c.487G>T
MANE Select
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NP_001079.1:p.Ala163Ser
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NR_110548.2:n.743G>T
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NM_001166579.2:c.622G>T
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NP_001160051.1:p.Ala208Ser
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