|
ENST00000356839.10:c.541C>T
MANE Select
|
ENSP00000349297.5:p.His181Tyr
|
|
|
ENST00000322910.9:c.*496C>T
|
ENSP00000325395.5:n.*496C>T
|
|
|
ENST00000350303.9:c.475C>T
|
ENSP00000344152.5:p.His159Tyr
|
|
|
ENST00000356839.9:c.541C>T
|
ENSP00000349297.5:p.His181Tyr
|
|
|
ENST00000543245.6:c.610C>T
|
ENSP00000438689.2:p.His204Tyr
|
|
|
ENST00000577191.5:n.618C>T
|
|
|
|
ENST00000577433.5:n.749C>T
|
|
|
|
ENST00000577857.5:n.357C>T
|
|
|
|
ENST00000579286.5:n.722C>T
|
|
|
|
ENST00000579886.2:c.379C>T
|
ENSP00000463246.1:p.His127Tyr
|
|
|
ENST00000580365.1:n.272C>T
|
|
|
|
ENST00000581378.5:c.259C>T
|
|
|
|
ENST00000581562.5:n.525-351C>T
|
|
|
|
ENST00000582166.1:n.522C>T
|
|
|
|
ENST00000583312.5:c.541C>T
|
ENSP00000467920.1:p.His181Tyr
|
|
|
ENST00000583760.1:n.323C>T
|
|
|
|
NM_000018.3:c.541C>T
|
NP_000009.1:p.His181Tyr
|
|
|
NM_001033859.2:c.475C>T
|
NP_001029031.1:p.His159Tyr
|
|
|
NM_001270447.1:c.610C>T
|
NP_001257376.1:p.His204Tyr
|
|
|
NM_001270448.1:c.313C>T
|
NP_001257377.1:p.His105Tyr
|
|
|
XM_006721516.2:c.541C>T
|
XP_006721579.2:p.His181Tyr
|
|
|
XM_011523829.1:c.541C>T
|
XP_011522131.1:p.His181Tyr
|
|
|
XM_011523830.1:c.541C>T
|
XP_011522132.1:p.His181Tyr
|
|
|
XR_934021.1:n.648C>T
|
|
|
|
XR_934022.1:n.648C>T
|
|
|
|
XR_934023.1:n.648C>T
|
|
|
|
XM_006721516.3:c.541C>T
|
XP_006721579.2:p.His181Tyr
|
|
|
XM_011523829.2:c.541C>T
|
XP_011522131.1:p.His181Tyr
|
|
|
XM_011523830.2:c.541C>T
|
XP_011522132.1:p.His181Tyr
|
|
|
XM_024450741.1:c.541C>T
|
XP_024306509.1:p.His181Tyr
|
|
|
XR_934021.2:n.600C>T
|
|
|
|
XR_934022.2:n.600C>T
|
|
|
|
XR_934023.2:n.600C>T
|
|
|
|
NM_000018.4:c.541C>T
MANE Select
|
NP_000009.1:p.His181Tyr
|
|
|
NM_001033859.3:c.475C>T
|
NP_001029031.1:p.His159Tyr
|
|
|
NM_001270447.2:c.610C>T
|
NP_001257376.1:p.His204Tyr
|
|
|
NM_001270448.2:c.313C>T
|
NP_001257377.1:p.His105Tyr
|
|
