ENST00000281961.3:c.652+4784T>C
MANE Select
|
ENSP00000281961.2:n.652+4784T>C
|
|
ENST00000281961.2:c.652+4784T>C
|
ENSP00000281961.2:n.652+4784T>C
|
|
ENST00000413011.5:n.371+4784T>C
|
|
|
ENST00000482239.5:n.395+4784T>C
|
|
|
ENST00000495402.1:n.431+4784T>C
|
|
|
ENST00000618232.1:c.*42-5040T>C
|
ENSP00000477622.1:n.*42-5040T>C
|
|
NM_001167959.1:c.106+4784T>C
|
NP_001161431.1:n.106+4784T>C
|
|
NM_152390.2:c.652+4784T>C
|
NP_689603.2:n.652+4784T>C
|
|
XM_005264144.1:c.515-5040T>C
|
XP_005264201.1:n.515-5040T>C
|
|
XM_005264145.1:c.401-5040T>C
|
XP_005264202.1:n.401-5040T>C
|
|
XM_017003369.1:c.*428T>C
|
XP_016858858.1:n.*428T>C
|
|
XM_017003370.2:c.106+4784T>C
|
XP_016858859.1:n.106+4784T>C
|
|
XM_017003371.1:c.106+4784T>C
|
XP_016858860.1:n.106+4784T>C
|
|
XM_024452702.1:c.401-23259T>C
|
XP_024308470.1:n.401-23259T>C
|
|
XM_024452703.1:c.106+4784T>C
|
XP_024308471.1:n.106+4784T>C
|
|
XM_024452704.1:c.106+4784T>C
|
XP_024308472.1:n.106+4784T>C
|
|
XM_024452705.1:c.106+4784T>C
|
XP_024308473.1:n.106+4784T>C
|
|
NM_152390.3:c.652+4784T>C
MANE Select
|
NP_689603.2:n.652+4784T>C
|
|
NM_001167959.2:c.106+4784T>C
|
NP_001161431.1:n.106+4784T>C
|
|