ENST00000683044.1:c.*1185A>C
|
ENSP00000507095.1:n.*1185A>C
|
|
ENST00000683288.1:c.*2113A>C
|
ENSP00000507477.1:n.*2113A>C
|
|
ENST00000683748.1:c.*17A>C
|
ENSP00000507377.1:n.*17A>C
|
|
ENST00000683905.1:c.*790A>C
|
ENSP00000506960.1:n.*790A>C
|
|
ENST00000684139.1:c.*17A>C
|
ENSP00000507295.1:n.*17A>C
|
|
ENST00000684210.1:n.1827A>C
|
|
|
ENST00000684314.1:c.*17A>C
|
ENSP00000507700.1:n.*17A>C
|
|
ENST00000684331.1:c.*834A>C
|
ENSP00000507431.1:n.*834A>C
|
|
ENST00000684463.1:n.752A>C
|
|
|
ENST00000684646.1:c.*17A>C
|
ENSP00000507723.1:n.*17A>C
|
|
ENST00000309971.9:c.*17A>C
MANE Select
|
ENSP00000308622.5:n.*17A>C
|
|
ENST00000309971.8:c.*17A>C
|
ENSP00000308622.4:n.*17A>C
|
|
NM_001003722.1:c.*17A>C , LRG_484t1:c.*17A>C
|
NP_001003722.1:n.*17A>C
|
|
XM_006717059.2:c.*17A>C
|
XP_006717122.1:n.*17A>C
|
|
XM_006717060.2:c.*17A>C
|
XP_006717123.1:n.*17A>C
|
|
XM_011518549.1:c.*17A>C
|
XP_011516851.1:n.*17A>C
|
|
XM_011518550.1:c.*17A>C
|
XP_011516852.1:n.*17A>C
|
|
XM_011518551.1:c.*17A>C
|
XP_011516853.1:n.*17A>C
|
|
XM_011518552.1:c.*17A>C
|
XP_011516854.1:n.*17A>C
|
|
XR_242681.3:n.100+2192T>G
|
|
|
XM_006717059.3:c.*17A>C
|
XP_006717122.1:n.*17A>C
|
|
XM_006717060.3:c.*17A>C
|
XP_006717123.1:n.*17A>C
|
|
XM_011518551.2:c.*17A>C
|
XP_011516853.1:n.*17A>C
|
|
XM_024447519.1:c.*17A>C
|
XP_024303287.1:n.*17A>C
|
|
NM_001003722.2:c.*17A>C
MANE Select
|
NP_001003722.1:n.*17A>C
|
|