ENST00000261937.11:c.2560G>T
MANE Select
|
ENSP00000261937.6:p.Gly854Cys
|
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ENST00000261937.10:c.2560G>T
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ENSP00000261937.6:p.Gly854Cys
|
|
ENST00000393347.7:c.2560G>T
|
ENSP00000377016.3:p.Gly854Cys
|
|
ENST00000502649.5:c.2560G>T
|
ENSP00000426057.1:p.Gly854Cys
|
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ENST00000507059.5:n.1655G>T
|
|
|
ENST00000619105.4:c.*1503G>T
|
ENSP00000481134.1:n.*1503G>T
|
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NM_002020.4:c.2560G>T
|
NP_002011.2:p.Gly854Cys
|
|
NM_182925.4:c.2560G>T
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NP_891555.2:p.Gly854Cys
|
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XM_011534477.1:c.2809G>T
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XP_011532779.1:p.Gly937Cys
|
|
XM_011534478.1:c.2791G>T
|
XP_011532780.1:p.Gly931Cys
|
|
XM_011534479.1:c.2809G>T
|
XP_011532781.1:p.Gly937Cys
|
|
XM_011534480.1:c.2809G>T
|
XP_011532782.1:p.Gly937Cys
|
|
XM_011534481.1:c.2809G>T
|
XP_011532783.1:p.Gly937Cys
|
|
XM_011534482.1:c.2578G>T
|
XP_011532784.1:p.Gly860Cys
|
|
XM_011534483.1:c.2500G>T
|
XP_011532785.1:p.Gly834Cys
|
|
XM_011534484.1:c.2101G>T
|
XP_011532786.1:p.Gly701Cys
|
|
XR_941095.1:n.2821G>T
|
|
|
NM_001354989.1:c.2560G>T
|
NP_001341918.1:p.Gly854Cys
|
|
XM_011534478.3:c.2791G>T
|
XP_011532780.1:p.Gly931Cys
|
|
XM_011534484.2:c.2101G>T
|
XP_011532786.1:p.Gly701Cys
|
|
XM_017009263.1:c.2791G>T
|
XP_016864752.1:p.Gly931Cys
|
|
XM_017009264.2:c.2791G>T
|
XP_016864753.1:p.Gly931Cys
|
|
XM_017009265.1:c.2791G>T
|
XP_016864754.1:p.Gly931Cys
|
|
XM_017009266.1:c.2791G>T
|
XP_016864755.1:p.Gly931Cys
|
|
XM_017009267.2:c.2791G>T
|
XP_016864756.1:p.Gly931Cys
|
|
XM_017009268.1:c.2482G>T
|
XP_016864757.1:p.Gly828Cys
|
|
XR_001742050.2:n.3025G>T
|
|
|
NM_182925.5:c.2560G>T
MANE Select
|
NP_891555.2:p.Gly854Cys
|
|
NM_001354989.2:c.2560G>T
|
NP_001341918.1:p.Gly854Cys
|
|
NM_002020.5:c.2560G>T
|
NP_002011.2:p.Gly854Cys
|
|