ENST00000305264.8:c.1217+362G>T
MANE Select
|
ENSP00000302967.3:n.1217+362G>T
|
|
ENST00000305264.7:c.1217+362G>T
|
ENSP00000302967.3:n.1217+362G>T
|
|
ENST00000459727.5:n.471+362G>T
|
|
|
ENST00000469207.5:n.216+362G>T
|
|
|
ENST00000469550.6:n.1290+362G>T
|
|
|
NM_003883.3:c.1217+362G>T
|
NP_003874.2:n.1217+362G>T
|
|
XM_011537697.1:c.656+362G>T
|
XP_011535999.1:n.656+362G>T
|
|
XR_427789.2:n.231-1001C>A
|
|
|
XR_944336.1:n.1302+362G>T
|
|
|
NM_001355040.1:c.758+362G>T
|
NP_001341969.1:n.758+362G>T
|
|
NM_001355041.1:c.656+362G>T
|
NP_001341970.1:n.656+362G>T
|
|
NR_149164.1:n.1203+362G>T
|
|
|
NR_149165.1:n.1165+362G>T
|
|
|
NR_149166.1:n.1081+362G>T
|
|
|
NR_149168.1:n.1308+362G>T
|
|
|
NR_149169.1:n.1228+362G>T
|
|
|
NM_003883.4:c.1217+362G>T
MANE Select
|
NP_003874.2:n.1217+362G>T
|
|
NM_001355040.2:c.758+362G>T
|
NP_001341969.1:n.758+362G>T
|
|
NM_001355041.2:c.656+362G>T
|
NP_001341970.1:n.656+362G>T
|
|
NR_149164.2:n.1196+362G>T
|
|
|
NR_149165.2:n.1158+362G>T
|
|
|
NR_149166.2:n.1074+362G>T
|
|
|
NR_149168.2:n.1301+362G>T
|
|
|
NR_149169.2:n.1221+362G>T
|
|
|