ENST00000322776.11:c.661G>C
MANE Select
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ENSP00000322450.6:p.Gly221Arg
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ENST00000647561.1:c.661G>C
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ENSP00000497587.1:p.Gly221Arg
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ENST00000322776.10:c.661G>C
|
ENSP00000322450.6:p.Gly221Arg
|
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ENST00000415352.6:c.640G>C
|
ENSP00000395368.2:p.Gly214Arg
|
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ENST00000526169.1:n.403G>C
|
|
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ENST00000526770.5:n.520G>C
|
|
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ENST00000529927.5:c.634G>C
|
ENSP00000436766.1:p.Gly212Arg
|
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ENST00000532244.5:c.358G>C
|
ENSP00000435202.1:p.Gly120Arg
|
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ENST00000532303.5:c.358G>C
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ENSP00000432015.1:p.Gly120Arg
|
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ENST00000533919.5:c.139G>C
|
ENSP00000435199.1:p.Gly47Arg
|
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NM_001166102.1:c.634G>C
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NP_001159574.1:p.Gly212Arg
|
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NM_007103.3:c.661G>C
|
NP_009034.2:p.Gly221Arg
|
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NM_001166102.2:c.634G>C
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NP_001159574.1:p.Gly212Arg
|
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NM_007103.4:c.661G>C
MANE Select
|
NP_009034.2:p.Gly221Arg
|
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