ENST00000356839.10:c.352G>C
MANE Select
|
ENSP00000349297.5:p.Asp118His
|
|
ENST00000322910.9:c.*307G>C
|
ENSP00000325395.5:n.*307G>C
|
|
ENST00000350303.9:c.286G>C
|
ENSP00000344152.5:p.Asp96His
|
|
ENST00000356839.9:c.352G>C
|
ENSP00000349297.5:p.Asp118His
|
|
ENST00000543245.6:c.421G>C
|
ENSP00000438689.2:p.Asp141His
|
|
ENST00000577191.5:n.429G>C
|
|
|
ENST00000577433.5:n.560G>C
|
|
|
ENST00000577857.5:n.293+103G>C
|
|
|
ENST00000579286.5:n.533G>C
|
|
|
ENST00000579886.2:c.202-12G>C
|
ENSP00000463246.1:n.202-12G>C
|
|
ENST00000580365.1:n.83G>C
|
|
|
ENST00000581378.5:c.51G>C
|
|
|
ENST00000581562.5:n.399G>C
|
|
|
ENST00000582056.5:n.535G>C
|
|
|
ENST00000582166.1:n.333G>C
|
|
|
ENST00000583312.5:c.352G>C
|
ENSP00000467920.1:p.Asp118His
|
|
ENST00000584103.5:c.385G>C
|
ENSP00000465353.1:p.Asp129His
|
|
NM_000018.3:c.352G>C
|
NP_000009.1:p.Asp118His
|
|
NM_001033859.2:c.286G>C
|
NP_001029031.1:p.Asp96His
|
|
NM_001270447.1:c.421G>C
|
NP_001257376.1:p.Asp141His
|
|
NM_001270448.1:c.124G>C
|
NP_001257377.1:p.Asp42His
|
|
XM_006721516.2:c.352G>C
|
XP_006721579.2:p.Asp118His
|
|
XM_011523829.1:c.352G>C
|
XP_011522131.1:p.Asp118His
|
|
XM_011523830.1:c.352G>C
|
XP_011522132.1:p.Asp118His
|
|
XR_934021.1:n.459G>C
|
|
|
XR_934022.1:n.459G>C
|
|
|
XR_934023.1:n.459G>C
|
|
|
XM_006721516.3:c.352G>C
|
XP_006721579.2:p.Asp118His
|
|
XM_011523829.2:c.352G>C
|
XP_011522131.1:p.Asp118His
|
|
XM_011523830.2:c.352G>C
|
XP_011522132.1:p.Asp118His
|
|
XM_024450741.1:c.352G>C
|
XP_024306509.1:p.Asp118His
|
|
XR_934021.2:n.411G>C
|
|
|
XR_934022.2:n.411G>C
|
|
|
XR_934023.2:n.411G>C
|
|
|
NM_000018.4:c.352G>C
MANE Select
|
NP_000009.1:p.Asp118His
|
|
NM_001033859.3:c.286G>C
|
NP_001029031.1:p.Asp96His
|
|
NM_001270447.2:c.421G>C
|
NP_001257376.1:p.Asp141His
|
|
NM_001270448.2:c.124G>C
|
NP_001257377.1:p.Asp42His
|
|