ENST00000379370.7:c.3977C=
MANE Select
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ENSP00000368678.2:p.Pro1326=
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|
ENST00000651234.1:c.3662C=
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ENSP00000499046.1:p.Pro1221=
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|
ENST00000652369.1:c.3662C=
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ENSP00000498543.1:p.Pro1221=
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|
ENST00000379370.6:c.3977C=
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ENSP00000368678.2:p.Pro1326=
|
|
ENST00000620552.4:c.3563C=
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ENSP00000484607.1:p.Pro1188=
|
|
NM_001305275.1:c.3977C=
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NP_001292204.1:p.Pro1326=
|
|
NM_198576.3:c.3977C=
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NP_940978.2:p.Pro1326=
|
|
XM_005244749.2:c.3977C=
|
XP_005244806.1:p.Pro1326=
|
|
XM_006710635.2:c.3977C=
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XP_006710698.1:p.Pro1326=
|
|
XM_011541429.1:c.3977C=
|
XP_011539731.1:p.Pro1326=
|
|
XM_011541430.1:c.3104C=
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XP_011539732.1:p.Pro1035=
|
|
XM_011541431.1:c.2243C=
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XP_011539733.1:p.Pro748=
|
|
XR_946650.1:n.4044C=
|
|
|
NM_001364727.1:c.3662C=
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NP_001351656.1:p.Pro1221=
|
|
XM_005244749.3:c.3977C=
|
XP_005244806.1:p.Pro1326=
|
|
XM_011541429.2:c.3977C=
|
XP_011539731.1:p.Pro1326=
|
|
XR_946650.2:n.4048C=
|
|
|
NM_001305275.2:c.3977C=
|
NP_001292204.1:p.Pro1326=
|
|
NM_198576.4:c.3977C=
MANE Select
|
NP_940978.2:p.Pro1326=
|
|
NM_001364727.2:c.3662C=
|
NP_001351656.1:p.Pro1221=
|
|