ENST00000532620.6:c.908G>A
MANE Select
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ENSP00000484252.1:p.Arg303Gln
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ENST00000532620.5:c.908G>A
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ENSP00000484252.1:p.Arg303Gln
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|
ENST00000534740.5:c.147+1911G>A
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ENSP00000482640.1:n.147+1911G>A
|
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ENST00000608857.2:c.908G>A
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ENSP00000477317.2:p.Arg303Gln
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NM_152762.2:c.908G>A
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NP_689975.2:p.Arg303Gln
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XM_011544887.1:c.908G>A
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XP_011543189.1:p.Arg303Gln
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XM_011544888.1:c.500G>A
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XP_011543190.1:p.Arg167Gln
|
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XR_949858.1:n.1139G>A
|
|
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XM_011544887.2:c.908G>A
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XP_011543189.1:p.Arg303Gln
|
|
XM_011544888.2:c.500G>A
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XP_011543190.1:p.Arg167Gln
|
|
NM_001395491.1:c.908G>A
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NP_001382420.1:p.Arg303Gln
|
|
NM_001395492.1:c.500G>A
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NP_001382421.1:p.Arg167Gln
|
|
NM_001395493.1:c.500G>A
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NP_001382422.1:p.Arg167Gln
|
|
NM_001395494.1:c.148-312G>A
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NP_001382423.1:n.148-312G>A
|
|
NM_001395495.1:c.119-268G>A
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NP_001382424.1:n.119-268G>A
|
|
NM_152762.3:c.908G>A
MANE Select
|
NP_689975.2:p.Arg303Gln
|
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NR_172563.1:n.343+1911G>A
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|
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