ENST00000399503.4:c.1847G>C
MANE Select
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ENSP00000382423.3:p.Gly616Ala
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ENST00000399503.3:c.1847G>C
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ENSP00000382423.3:p.Gly616Ala
|
|
NM_005921.1:c.1847G>C
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NP_005912.1:p.Gly616Ala
|
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XM_005248519.3:c.1469G>C
|
XP_005248576.2:p.Gly490Ala
|
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XM_011543406.1:c.1592G>C
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XP_011541708.1:p.Gly531Ala
|
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XM_011543407.1:c.1686+2187G>C
|
XP_011541709.1:n.1686+2187G>C
|
|
XM_011543408.1:c.1847G>C
|
XP_011541710.1:p.Gly616Ala
|
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XM_017009484.1:c.1436G>C
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XP_016864973.1:p.Gly479Ala
|
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XM_017009485.1:c.1358G>C
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XP_016864974.1:p.Gly453Ala
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XR_001742068.2:n.1878G>C
|
|
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NM_005921.2:c.1847G>C
MANE Select
|
NP_005912.1:p.Gly616Ala
|
|