ENST00000341947.7:c.3713A>C
MANE Select
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ENSP00000339915.2:p.Glu1238Ala
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ENST00000341947.6:c.3713A>C
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ENSP00000339915.2:p.Glu1238Ala
|
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ENST00000361917.5:c.3392A>C
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ENSP00000355123.1:p.Glu1131Ala
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ENST00000374708.8:c.3455A>C
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ENSP00000363840.4:p.Glu1152Ala
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ENST00000477772.1:n.273-3652A>C
|
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NM_080679.2:c.3392A>C
|
NP_542410.2:p.Glu1131Ala
|
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NM_080680.2:c.3713A>C
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NP_542411.2:p.Glu1238Ala
|
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NM_080681.2:c.3455A>C
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NP_542412.2:p.Glu1152Ala
|
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XM_011514298.1:c.2867A>C
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XP_011512600.1:p.Glu956Ala
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XM_011514299.1:c.2999A>C
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XP_011512601.1:p.Glu1000Ala
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XM_011514300.1:c.2819A>C
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XP_011512602.1:p.Glu940Ala
|
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XM_011514301.1:c.2756A>C
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XP_011512603.1:p.Glu919Ala
|
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XM_011514302.1:c.2600A>C
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XP_011512604.1:p.Glu867Ala
|
|
XM_011514299.2:c.2999A>C
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XP_011512601.1:p.Glu1000Ala
|
|
XM_011514300.2:c.2819A>C
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XP_011512602.1:p.Glu940Ala
|
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XM_011514302.2:c.2600A>C
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XP_011512604.1:p.Glu867Ala
|
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XM_017010250.1:c.3713A>C
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XP_016865739.1:p.Glu1238Ala
|
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XM_017010251.2:c.2531A>C
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XP_016865740.1:p.Glu844Ala
|
|
NM_080680.3:c.3713A>C
MANE Select
|
NP_542411.2:p.Glu1238Ala
|
|
NM_080681.3:c.3455A>C
|
NP_542412.2:p.Glu1152Ala
|
|
NM_080679.3:c.3392A>C
|
NP_542410.2:p.Glu1131Ala
|
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