ENST00000683044.1:c.*1099+326A>T
|
ENSP00000507095.1:n.*1099+326A>T
|
|
ENST00000683288.1:c.*2027+326A>T
|
ENSP00000507477.1:n.*2027+326A>T
|
|
ENST00000683748.1:c.2055+326A>T
|
ENSP00000507377.1:n.2055+326A>T
|
|
ENST00000683905.1:c.*704+326A>T
|
ENSP00000506960.1:n.*704+326A>T
|
|
ENST00000684139.1:c.1563+326A>T
|
ENSP00000507295.1:n.1563+326A>T
|
|
ENST00000684210.1:n.1741+326A>T
|
|
|
ENST00000684314.1:c.1923+326A>T
|
ENSP00000507700.1:n.1923+326A>T
|
|
ENST00000684331.1:c.*311A>T
|
ENSP00000507431.1:n.*311A>T
|
|
ENST00000684463.1:n.666+326A>T
|
|
|
ENST00000684646.1:c.1815+326A>T
|
ENSP00000507723.1:n.1815+326A>T
|
|
ENST00000309971.9:c.2028+326A>T
MANE Select
|
ENSP00000308622.5:n.2028+326A>T
|
|
ENST00000309971.8:c.2028+326A>T
|
ENSP00000308622.4:n.2028+326A>T
|
|
NM_001003722.1:c.2028+326A>T , LRG_484t1:c.2028+326A>T
|
NP_001003722.1:n.2028+326A>T
|
|
XM_006717059.2:c.2064+326A>T
|
XP_006717122.1:n.2064+326A>T
|
|
XM_006717060.2:c.2037+326A>T
|
XP_006717123.1:n.2037+326A>T
|
|
XM_011518549.1:c.2064+326A>T
|
XP_011516851.1:n.2064+326A>T
|
|
XM_011518550.1:c.2064+326A>T
|
XP_011516852.1:n.2064+326A>T
|
|
XM_011518551.1:c.2055+326A>T
|
XP_011516853.1:n.2055+326A>T
|
|
XM_011518552.1:c.1305+326A>T
|
XP_011516854.1:n.1305+326A>T
|
|
XR_242681.3:n.100+2715T>A
|
|
|
XR_428600.2:n.124+306T>A
|
|
|
XM_006717059.3:c.2064+326A>T
|
XP_006717122.1:n.2064+326A>T
|
|
XM_006717060.3:c.2037+326A>T
|
XP_006717123.1:n.2037+326A>T
|
|
XM_011518551.2:c.2055+326A>T
|
XP_011516853.1:n.2055+326A>T
|
|
XM_024447519.1:c.2037+326A>T
|
XP_024303287.1:n.2037+326A>T
|
|
XR_428600.3:n.126+306T>A
|
|
|
NM_001003722.2:c.2028+326A>T
MANE Select
|
NP_001003722.1:n.2028+326A>T
|
|