ENST00000273064.11:c.285A>C
MANE Select
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ENSP00000273064.6:p.Ala95=
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ENST00000273064.10:c.285A>C
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ENSP00000273064.6:p.Ala95=
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|
ENST00000295701.9:c.285A>C
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ENSP00000295701.5:p.Ala95=
|
|
ENST00000432877.5:c.*177A>C
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ENSP00000392394.1:n.*177A>C
|
|
ENST00000542068.5:c.285A>C
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ENSP00000443687.1:p.Ala95=
|
|
ENST00000627282.2:c.285A>C
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ENSP00000486540.1:p.Ala95=
|
|
NM_001271634.1:c.285A>C
|
NP_001258563.1:p.Ala95=
|
|
NM_001271635.1:c.285A>C
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NP_001258564.1:p.Ala95=
|
|
NM_005444.2:c.285A>C
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NP_005435.1:p.Ala95=
|
|
NR_073390.1:n.660A>C
|
|
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XM_011512138.1:c.126A>C
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XP_011510440.1:p.Ala42=
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|
XM_011512138.3:c.126A>C
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XP_011510440.1:p.Ala42=
|
|
XM_017005248.1:c.123A>C
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XP_016860737.1:p.Ala41=
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|
XM_017005249.2:c.126A>C
|
XP_016860738.1:p.Ala42=
|
|
NM_001271634.2:c.285A>C
|
NP_001258563.1:p.Ala95=
|
|
NM_005444.3:c.285A>C
MANE Select
|
NP_005435.1:p.Ala95=
|
|
NR_073390.2:n.401A>C
|
|
|
NM_001271635.2:c.285A>C
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NP_001258564.1:p.Ala95=
|
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