ENST00000379370.7:c.5112C=
MANE Select
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ENSP00000368678.2:p.Tyr1704=
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ENST00000651234.1:c.4797C=
|
ENSP00000499046.1:p.Tyr1599=
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ENST00000652369.1:c.4797C=
|
ENSP00000498543.1:p.Tyr1599=
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ENST00000379370.6:c.5112C=
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ENSP00000368678.2:p.Tyr1704=
|
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ENST00000419249.1:c.7C=
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|
|
ENST00000620552.4:c.4698C=
|
ENSP00000484607.1:p.Tyr1566=
|
|
NM_001305275.1:c.5112C=
|
NP_001292204.1:p.Tyr1704=
|
|
NM_198576.3:c.5112C=
|
NP_940978.2:p.Tyr1704=
|
|
XM_005244749.2:c.5112C=
|
XP_005244806.1:p.Tyr1704=
|
|
XM_006710635.2:c.5112C=
|
XP_006710698.1:p.Tyr1704=
|
|
XM_011541429.1:c.5112C=
|
XP_011539731.1:p.Tyr1704=
|
|
XM_011541430.1:c.4239C=
|
XP_011539732.1:p.Tyr1413=
|
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XM_011541431.1:c.3378C=
|
XP_011539733.1:p.Tyr1126=
|
|
XR_946650.1:n.5179C=
|
|
|
NM_001364727.1:c.4797C=
|
NP_001351656.1:p.Tyr1599=
|
|
XM_005244749.3:c.5112C=
|
XP_005244806.1:p.Tyr1704=
|
|
XM_011541429.2:c.5112C=
|
XP_011539731.1:p.Tyr1704=
|
|
XR_946650.2:n.5183C=
|
|
|
NM_001305275.2:c.5112C=
|
NP_001292204.1:p.Tyr1704=
|
|
NM_198576.4:c.5112C=
MANE Select
|
NP_940978.2:p.Tyr1704=
|
|
NM_001364727.2:c.4797C=
|
NP_001351656.1:p.Tyr1599=
|
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