ENST00000294304.12:c.1801+128A>G
MANE Select
|
ENSP00000294304.6:n.1801+128A>G
|
|
ENST00000294304.11:c.1801+128A>G
|
ENSP00000294304.6:n.1801+128A>G
|
|
ENST00000529993.5:c.*213+128A>G
|
ENSP00000436652.1:n.*213+128A>G
|
|
NM_001291902.1:c.-137+128A>G
|
NP_001278831.1:n.-137+128A>G
|
|
NM_002335.3:c.1801+128A>G
|
NP_002326.2:n.1801+128A>G
|
|
XM_005273994.2:c.1801+128A>G
|
XP_005274051.1:n.1801+128A>G
|
|
XM_011545029.1:c.1828+128A>G
|
XP_011543331.1:n.1828+128A>G
|
|
XM_011545030.1:c.1828+128A>G
|
XP_011543332.1:n.1828+128A>G
|
|
XM_011545031.1:c.1828+128A>G
|
XP_011543333.1:n.1828+128A>G
|
|
XR_949925.1:n.1843+128A>G
|
|
|
XR_949926.1:n.1843+128A>G
|
|
|
XR_001747874.1:n.1843+128A>G
|
|
|
XR_949925.2:n.1843+128A>G
|
|
|
XR_949926.2:n.1843+128A>G
|
|
|
NM_002335.4:c.1801+128A>G
MANE Select
|
NP_002326.2:n.1801+128A>G
|
|
NM_001291902.2:c.-137+128A>G
|
NP_001278831.1:n.-137+128A>G
|
|