|
ENST00000356839.10:c.601T>C
MANE Select
|
ENSP00000349297.5:p.Tyr201His
|
|
|
ENST00000322910.9:c.*556T>C
|
ENSP00000325395.5:n.*556T>C
|
|
|
ENST00000350303.9:c.535T>C
|
ENSP00000344152.5:p.Tyr179His
|
|
|
ENST00000356839.9:c.601T>C
|
ENSP00000349297.5:p.Tyr201His
|
|
|
ENST00000543245.6:c.670T>C
|
ENSP00000438689.2:p.Tyr224His
|
|
|
ENST00000577191.5:n.678T>C
|
|
|
|
ENST00000577857.5:n.417T>C
|
|
|
|
ENST00000579286.5:n.782T>C
|
|
|
|
ENST00000579886.2:c.439T>C
|
ENSP00000463246.1:p.Tyr147His
|
|
|
ENST00000580365.1:n.332T>C
|
|
|
|
ENST00000581378.5:c.319T>C
|
|
|
|
ENST00000581562.5:n.525-291T>C
|
|
|
|
ENST00000583312.5:c.601T>C
|
ENSP00000467920.1:p.Tyr201His
|
|
|
ENST00000583760.1:n.383T>C
|
|
|
|
NM_000018.3:c.601T>C
|
NP_000009.1:p.Tyr201His
|
|
|
NM_001033859.2:c.535T>C
|
NP_001029031.1:p.Tyr179His
|
|
|
NM_001270447.1:c.670T>C
|
NP_001257376.1:p.Tyr224His
|
|
|
NM_001270448.1:c.373T>C
|
NP_001257377.1:p.Tyr125His
|
|
|
XM_006721516.2:c.601T>C
|
XP_006721579.2:p.Tyr201His
|
|
|
XM_011523829.1:c.601T>C
|
XP_011522131.1:p.Tyr201His
|
|
|
XM_011523830.1:c.601T>C
|
XP_011522132.1:p.Tyr201His
|
|
|
XR_934021.1:n.708T>C
|
|
|
|
XR_934022.1:n.708T>C
|
|
|
|
XR_934023.1:n.708T>C
|
|
|
|
XM_006721516.3:c.601T>C
|
XP_006721579.2:p.Tyr201His
|
|
|
XM_011523829.2:c.601T>C
|
XP_011522131.1:p.Tyr201His
|
|
|
XM_011523830.2:c.601T>C
|
XP_011522132.1:p.Tyr201His
|
|
|
XM_024450741.1:c.601T>C
|
XP_024306509.1:p.Tyr201His
|
|
|
XR_934021.2:n.660T>C
|
|
|
|
XR_934022.2:n.660T>C
|
|
|
|
XR_934023.2:n.660T>C
|
|
|
|
NM_000018.4:c.601T>C
MANE Select
|
NP_000009.1:p.Tyr201His
|
|
|
NM_001033859.3:c.535T>C
|
NP_001029031.1:p.Tyr179His
|
|
|
NM_001270447.2:c.670T>C
|
NP_001257376.1:p.Tyr224His
|
|
|
NM_001270448.2:c.373T>C
|
NP_001257377.1:p.Tyr125His
|
|
