ENST00000261937.11:c.3244G>T
MANE Select
|
ENSP00000261937.6:p.Ala1082Ser
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ENST00000261937.10:c.3244G>T
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ENSP00000261937.6:p.Ala1082Ser
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|
ENST00000393347.7:c.3244G>T
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ENSP00000377016.3:p.Ala1082Ser
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|
ENST00000502649.5:c.3244G>T
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ENSP00000426057.1:p.Ala1082Ser
|
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ENST00000507059.5:n.2637G>T
|
|
|
ENST00000512795.1:c.358G>T
|
ENSP00000421535.1:p.Ala120Ser
|
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ENST00000514810.1:n.611G>T
|
|
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ENST00000619105.4:c.*2187G>T
|
ENSP00000481134.1:n.*2187G>T
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|
NM_002020.4:c.3244G>T
|
NP_002011.2:p.Ala1082Ser
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|
NM_182925.4:c.3244G>T
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NP_891555.2:p.Ala1082Ser
|
|
XM_011534477.1:c.3493G>T
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XP_011532779.1:p.Ala1165Ser
|
|
XM_011534478.1:c.3475G>T
|
XP_011532780.1:p.Ala1159Ser
|
|
XM_011534479.1:c.3493G>T
|
XP_011532781.1:p.Ala1165Ser
|
|
XM_011534480.1:c.3493G>T
|
XP_011532782.1:p.Ala1165Ser
|
|
XM_011534481.1:c.3493G>T
|
XP_011532783.1:p.Ala1165Ser
|
|
XM_011534482.1:c.3262G>T
|
XP_011532784.1:p.Ala1088Ser
|
|
XM_011534483.1:c.3184G>T
|
XP_011532785.1:p.Ala1062Ser
|
|
XM_011534484.1:c.2785G>T
|
XP_011532786.1:p.Ala929Ser
|
|
XR_941095.1:n.3505G>T
|
|
|
NM_001354989.1:c.3244G>T
|
NP_001341918.1:p.Ala1082Ser
|
|
XM_011534478.3:c.3475G>T
|
XP_011532780.1:p.Ala1159Ser
|
|
XM_011534484.2:c.2785G>T
|
XP_011532786.1:p.Ala929Ser
|
|
XM_017009263.1:c.3475G>T
|
XP_016864752.1:p.Ala1159Ser
|
|
XM_017009264.2:c.3475G>T
|
XP_016864753.1:p.Ala1159Ser
|
|
XM_017009265.1:c.3475G>T
|
XP_016864754.1:p.Ala1159Ser
|
|
XM_017009266.1:c.3475G>T
|
XP_016864755.1:p.Ala1159Ser
|
|
XM_017009267.2:c.3475G>T
|
XP_016864756.1:p.Ala1159Ser
|
|
XM_017009268.1:c.3166G>T
|
XP_016864757.1:p.Ala1056Ser
|
|
XR_001742050.2:n.3709G>T
|
|
|
NM_182925.5:c.3244G>T
MANE Select
|
NP_891555.2:p.Ala1082Ser
|
|
NM_001354989.2:c.3244G>T
|
NP_001341918.1:p.Ala1082Ser
|
|
NM_002020.5:c.3244G>T
|
NP_002011.2:p.Ala1082Ser
|
|