ENST00000682850.1:c.-447T>C
MANE Select
|
ENSP00000508024.1:n.-447T>C
|
|
ENST00000558573.1:n.104T>C
|
|
|
XM_011521338.1:c.-447T>C
|
XP_011519640.1:n.-447T>C
|
|
XM_011521339.1:c.-328T>C
|
XP_011519641.1:n.-328T>C
|
|
XM_011521340.1:c.-269T>C
|
XP_011519642.1:n.-269T>C
|
|
XM_011521343.1:c.-531T>C
|
XP_011519645.1:n.-531T>C
|
|
XM_011521345.1:c.-502T>C
|
XP_011519647.1:n.-502T>C
|
|
XM_011521338.3:c.-447T>C
|
XP_011519640.1:n.-447T>C
|
|
XM_011521339.3:c.-328T>C
|
XP_011519641.1:n.-328T>C
|
|
XM_011521340.3:c.-269T>C
|
XP_011519642.1:n.-269T>C
|
|
XM_011521343.3:c.-531T>C
|
XP_011519645.1:n.-531T>C
|
|
XM_011521345.3:c.-502T>C
|
XP_011519647.1:n.-502T>C
|
|
NM_001387260.1:c.-76+119T>C
|
NP_001374189.1:n.-76+119T>C
|
|
NM_001387261.1:c.-269T>C
|
NP_001374190.1:n.-269T>C
|
|
NM_001387262.1:c.-537T>C
|
NP_001374191.1:n.-537T>C
|
|
NM_001387263.1:c.-447T>C
MANE Select
|
NP_001374192.1:n.-447T>C
|
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