ENST00000231749.8:c.559G>T
MANE Select
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ENSP00000231749.3:p.Ala187Ser
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ENST00000231749.7:c.559G>T
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ENSP00000231749.3:p.Ala187Ser
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ENST00000360165.7:c.559G>T
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ENSP00000353289.3:p.Ala187Ser
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ENST00000442887.1:c.430G>T
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ENSP00000393687.1:p.Ala144Ser
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ENST00000443080.5:c.*311G>T
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ENSP00000415661.1:n.*311G>T
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ENST00000475688.1:n.11G>T
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|
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NM_001308379.1:c.559G>T
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NP_001295308.1:p.Ala187Ser
|
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NM_015896.2:c.559G>T
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NP_056980.2:p.Ala187Ser
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NM_015896.3:c.559G>T
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NP_056980.2:p.Ala187Ser
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XM_005265216.2:c.322G>T
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XP_005265273.1:p.Ala108Ser
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XM_005265216.3:c.322G>T
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XP_005265273.1:p.Ala108Ser
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NM_015896.4:c.559G>T
MANE Select
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NP_056980.2:p.Ala187Ser
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NM_001308379.2:c.559G>T
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NP_001295308.1:p.Ala187Ser
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