ENST00000399503.4:c.2604C=
MANE Select
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ENSP00000382423.3:p.Ala868=
|
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ENST00000399503.3:c.2604C=
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ENSP00000382423.3:p.Ala868=
|
|
NM_005921.1:c.2604C=
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NP_005912.1:p.Ala868=
|
|
XM_005248519.3:c.2226C=
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XP_005248576.2:p.Ala742=
|
|
XM_011543406.1:c.2349C=
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XP_011541708.1:p.Ala783=
|
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XM_011543407.1:c.2325C=
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XP_011541709.1:p.Ala775=
|
|
XM_011543408.1:c.2604C=
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XP_011541710.1:p.Ala868=
|
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XM_017009484.1:c.2193C=
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XP_016864973.1:p.Ala731=
|
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XM_017009485.1:c.2115C=
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XP_016864974.1:p.Ala705=
|
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XR_001742068.2:n.2635C=
|
|
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NM_005921.2:c.2604C=
MANE Select
|
NP_005912.1:p.Ala868=
|
|