ENST00000260197.12:c.3556T>G
MANE Select
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ENSP00000260197.6:p.Trp1186Gly
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ENST00000260197.11:c.3556T>G
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ENSP00000260197.6:p.Trp1186Gly
|
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ENST00000525532.5:c.388T>G
|
ENSP00000434634.1:p.Trp130Gly
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ENST00000532694.5:c.94T>G
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ENSP00000432131.1:p.Trp32Gly
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ENST00000534286.5:c.286T>G
|
ENSP00000436447.1:p.Trp96Gly
|
|
NM_003105.5:c.3556T>G
|
NP_003096.1:p.Trp1186Gly
|
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XM_011542963.1:c.3442T>G
|
XP_011541265.1:p.Trp1148Gly
|
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XM_011542964.1:c.3556T>G
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XP_011541266.1:p.Trp1186Gly
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XM_011542965.1:c.2017T>G
|
XP_011541267.1:p.Trp673Gly
|
|
XM_011542966.1:c.916T>G
|
XP_011541268.1:p.Trp306Gly
|
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XM_011542967.1:c.388T>G
|
XP_011541269.1:p.Trp130Gly
|
|
XM_011542963.3:c.3442T>G
|
XP_011541265.1:p.Trp1148Gly
|
|
XM_011542965.3:c.2017T>G
|
XP_011541267.1:p.Trp673Gly
|
|
XM_011542967.3:c.388T>G
|
XP_011541269.1:p.Trp130Gly
|
|
XM_017018169.2:c.3244T>G
|
XP_016873658.1:p.Trp1082Gly
|
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XM_017018170.2:c.3031T>G
|
XP_016873659.1:p.Trp1011Gly
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XM_017018171.1:c.3556T>G
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XP_016873660.1:p.Trp1186Gly
|
|
XM_017018172.2:c.916T>G
|
XP_016873661.1:p.Trp306Gly
|
|
NM_003105.6:c.3556T>G
MANE Select
|
NP_003096.2:p.Trp1186Gly
|
|