ENST00000260197.12:c.1414G>T
MANE Select
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ENSP00000260197.6:p.Gly472Cys
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ENST00000260197.11:c.1414G>T
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ENSP00000260197.6:p.Gly472Cys
|
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ENST00000532451.1:n.1366G>T
|
|
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NM_003105.5:c.1414G>T
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NP_003096.1:p.Gly472Cys
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XM_011542963.1:c.1414G>T
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XP_011541265.1:p.Gly472Cys
|
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XM_011542964.1:c.1414G>T
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XP_011541266.1:p.Gly472Cys
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XM_011542965.1:c.-209G>T
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XP_011541267.1:n.-209G>T
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XM_011542963.3:c.1414G>T
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XP_011541265.1:p.Gly472Cys
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XM_011542965.3:c.-209G>T
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XP_011541267.1:n.-209G>T
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XM_017018169.2:c.1102G>T
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XP_016873658.1:p.Gly368Cys
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XM_017018170.2:c.889G>T
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XP_016873659.1:p.Gly297Cys
|
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XM_017018171.1:c.1414G>T
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XP_016873660.1:p.Gly472Cys
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NM_003105.6:c.1414G>T
MANE Select
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NP_003096.2:p.Gly472Cys
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