ENST00000379370.7:c.1878C=
MANE Select
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ENSP00000368678.2:p.Pro626=
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|
ENST00000651234.1:c.1563C=
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ENSP00000499046.1:p.Pro521=
|
|
ENST00000652369.1:c.1563C=
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ENSP00000498543.1:p.Pro521=
|
|
ENST00000379370.6:c.1878C=
|
ENSP00000368678.2:p.Pro626=
|
|
ENST00000620552.4:c.1464C=
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ENSP00000484607.1:p.Pro488=
|
|
NM_001305275.1:c.1878C=
|
NP_001292204.1:p.Pro626=
|
|
NM_198576.3:c.1878C=
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NP_940978.2:p.Pro626=
|
|
XM_005244749.2:c.1878C=
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XP_005244806.1:p.Pro626=
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|
XM_006710635.2:c.1878C=
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XP_006710698.1:p.Pro626=
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|
XM_011541429.1:c.1878C=
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XP_011539731.1:p.Pro626=
|
|
XM_011541430.1:c.1005C=
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XP_011539732.1:p.Pro335=
|
|
XM_011541431.1:c.144C=
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XP_011539733.1:p.Pro48=
|
|
XR_946650.1:n.1945C=
|
|
|
NM_001364727.1:c.1563C=
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NP_001351656.1:p.Pro521=
|
|
XM_005244749.3:c.1878C=
|
XP_005244806.1:p.Pro626=
|
|
XM_011541429.2:c.1878C=
|
XP_011539731.1:p.Pro626=
|
|
XR_946650.2:n.1949C=
|
|
|
NM_001305275.2:c.1878C=
|
NP_001292204.1:p.Pro626=
|
|
NM_198576.4:c.1878C=
MANE Select
|
NP_940978.2:p.Pro626=
|
|
NM_001364727.2:c.1563C=
|
NP_001351656.1:p.Pro521=
|
|