ENST00000294304.12:c.4489-69G>T
MANE Select
|
ENSP00000294304.6:n.4489-69G>T
|
|
ENST00000294304.11:c.4489-69G>T
|
ENSP00000294304.6:n.4489-69G>T
|
|
ENST00000529702.1:c.159-69G>T
|
|
|
ENST00000529993.5:c.*3095-69G>T
|
ENSP00000436652.1:n.*3095-69G>T
|
|
NM_001291902.1:c.2746-69G>T
|
NP_001278831.1:n.2746-69G>T
|
|
NM_002335.3:c.4489-69G>T
|
NP_002326.2:n.4489-69G>T
|
|
XM_005273994.2:c.4603-69G>T
|
XP_005274051.1:n.4603-69G>T
|
|
XM_011545029.1:c.4630-69G>T
|
XP_011543331.1:n.4630-69G>T
|
|
XM_011545030.1:c.4516-69G>T
|
XP_011543332.1:n.4516-69G>T
|
|
XM_011545031.1:c.4646-69G>T
|
XP_011543333.1:n.4646-69G>T
|
|
XR_949925.1:n.4645-69G>T
|
|
|
XR_949926.1:n.4661-69G>T
|
|
|
XM_017017735.1:c.2860-69G>T
|
XP_016873224.1:n.2860-69G>T
|
|
XM_017017736.1:c.2143-69G>T
|
XP_016873225.1:n.2143-69G>T
|
|
XR_949925.2:n.4645-69G>T
|
|
|
XR_949926.2:n.4661-69G>T
|
|
|
NM_002335.4:c.4489-69G>T
MANE Select
|
NP_002326.2:n.4489-69G>T
|
|
NM_001291902.2:c.2746-69G>T
|
NP_001278831.1:n.2746-69G>T
|
|