ENST00000233202.11:c.1651T>C
MANE Select
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ENSP00000233202.6:p.Ter551Gln
|
|
ENST00000233202.10:c.1651T>C
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ENSP00000233202.6:p.Ter551Gln
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|
ENST00000354352.9:c.*1233T>C
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ENSP00000346320.5:n.*1233T>C
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ENST00000465984.5:n.2127T>C
|
|
|
ENST00000468221.5:n.4778T>C
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|
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NM_000578.3:c.1651T>C
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NP_000569.3:p.Ter551Gln
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|
XM_005246793.2:c.1450T>C
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XP_005246850.1:p.Ter484Gln
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|
XM_005246794.2:c.1297T>C
|
XP_005246851.1:p.Ter433Gln
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|
XM_006712709.2:c.1297T>C
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XP_006712772.1:p.Ter433Gln
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|
XM_006712710.2:c.1297T>C
|
XP_006712773.1:p.Ter433Gln
|
|
XM_006712711.2:c.1204T>C
|
XP_006712774.1:p.Ter402Gln
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|
XM_011511684.1:c.1324T>C
|
XP_011509986.1:p.Ter442Gln
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|
XM_011511685.1:c.1324T>C
|
XP_011509987.1:p.Ter442Gln
|
|
XM_005246793.4:c.1450T>C
|
XP_005246850.1:p.Ter484Gln
|
|
XM_005246794.4:c.1297T>C
|
XP_005246851.1:p.Ter433Gln
|
|
XM_006712709.4:c.1297T>C
|
XP_006712772.1:p.Ter433Gln
|
|
XM_006712710.4:c.1297T>C
|
XP_006712773.1:p.Ter433Gln
|
|
XM_006712711.4:c.1204T>C
|
XP_006712774.1:p.Ter402Gln
|
|
XM_011511684.3:c.1324T>C
|
XP_011509986.1:p.Ter442Gln
|
|
XM_011511685.3:c.1324T>C
|
XP_011509987.1:p.Ter442Gln
|
|
XM_017004765.2:c.1528T>C
|
XP_016860254.1:p.Ter510Gln
|
|
XM_017004766.2:c.1450T>C
|
XP_016860255.1:p.Ter484Gln
|
|
XM_017004767.2:c.1282T>C
|
XP_016860256.1:p.Ter428Gln
|
|
XR_427107.3:n.2666T>C
|
|
|
XR_427108.4:n.2977T>C
|
|
|
NM_000578.4:c.1651T>C
MANE Select
|
NP_000569.3:p.Ter551Gln
|
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