ENST00000356839.10:c.1846G>C
MANE Select
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ENSP00000349297.5:p.Glu616Gln
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ENST00000322910.9:c.*1801G>C
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ENSP00000325395.5:n.*1801G>C
|
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ENST00000350303.9:c.1780G>C
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ENSP00000344152.5:p.Glu594Gln
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ENST00000356839.9:c.1846G>C
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ENSP00000349297.5:p.Glu616Gln
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ENST00000542255.6:c.725G>C
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|
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ENST00000543245.6:c.1915G>C
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ENSP00000438689.2:p.Glu639Gln
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ENST00000578033.1:n.271G>C
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ENST00000578319.5:n.427G>C
|
|
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ENST00000578711.1:n.1471G>C
|
|
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ENST00000578809.5:n.418G>C
|
|
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ENST00000579425.5:n.962G>C
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|
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ENST00000579546.1:c.581G>C
|
|
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ENST00000583848.5:c.212G>C
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ENSP00000466487.1:n.212G>C
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ENST00000583850.5:n.617G>C
|
|
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ENST00000583858.5:c.777G>C
|
|
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NM_000018.3:c.1846G>C
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NP_000009.1:p.Glu616Gln
|
|
NM_001033859.2:c.1780G>C
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NP_001029031.1:p.Glu594Gln
|
|
NM_001270447.1:c.1915G>C
|
NP_001257376.1:p.Glu639Gln
|
|
NM_001270448.1:c.1618G>C
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NP_001257377.1:p.Glu540Gln
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XM_006721516.2:c.1867G>C
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XP_006721579.2:p.Glu623Gln
|
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XM_011523829.1:c.1765G>C
|
XP_011522131.1:p.Glu589Gln
|
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XM_011523830.1:c.1744G>C
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XP_011522132.1:p.Glu582Gln
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XR_934021.1:n.1949G>C
|
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XR_934022.1:n.1855G>C
|
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XR_934023.1:n.1876G>C
|
|
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XM_006721516.3:c.1867G>C
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XP_006721579.2:p.Glu623Gln
|
|
XM_011523829.2:c.1765G>C
|
XP_011522131.1:p.Glu589Gln
|
|
XM_011523830.2:c.1744G>C
|
XP_011522132.1:p.Glu582Gln
|
|
XM_024450741.1:c.1834G>C
|
XP_024306509.1:p.Glu612Gln
|
|
XR_934021.2:n.1901G>C
|
|
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XR_934022.2:n.1807G>C
|
|
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XR_934023.2:n.1828G>C
|
|
|
NM_000018.4:c.1846G>C
MANE Select
|
NP_000009.1:p.Glu616Gln
|
|
NM_001033859.3:c.1780G>C
|
NP_001029031.1:p.Glu594Gln
|
|
NM_001270447.2:c.1915G>C
|
NP_001257376.1:p.Glu639Gln
|
|
NM_001270448.2:c.1618G>C
|
NP_001257377.1:p.Glu540Gln
|
|