ENST00000379644.9:c.1727-34G>C
MANE Select
|
ENSP00000368965.4:n.1727-34G>C
|
|
ENST00000379644.8:c.1727-34G>C
|
ENSP00000368965.4:n.1727-34G>C
|
|
ENST00000519705.1:n.1043-34G>C
|
|
|
ENST00000521576.1:c.878-34G>C
|
ENSP00000429029.1:n.878-34G>C
|
|
NM_152419.2:c.1727-34G>C
|
NP_689632.2:n.1727-34G>C
|
|
XM_005273409.1:c.1838-34G>C
|
XP_005273466.1:n.1838-34G>C
|
|
XM_005273410.1:c.1814-34G>C
|
XP_005273467.1:n.1814-34G>C
|
|
XM_005273411.1:c.1646-34G>C
|
XP_005273468.1:n.1646-34G>C
|
|
NM_001363227.1:c.1814-34G>C
|
NP_001350156.1:n.1814-34G>C
|
|
NM_001363228.1:c.1535-34G>C
|
NP_001350157.1:n.1535-34G>C
|
|
NM_001363229.1:c.863-34G>C
|
NP_001350158.1:n.863-34G>C
|
|
NM_152419.3:c.1727-34G>C
MANE Select
|
NP_689632.2:n.1727-34G>C
|
|
NM_001363227.2:c.1814-34G>C
|
NP_001350156.1:n.1814-34G>C
|
|
NM_001363228.2:c.1535-34G>C
|
NP_001350157.1:n.1535-34G>C
|
|
NM_001363229.2:c.863-34G>C
|
NP_001350158.1:n.863-34G>C
|
|