ENST00000259455.4:c.1893+21394C>T
MANE Select
|
ENSP00000259455.2:n.1893+21394C>T
|
|
ENST00000637410.1:n.1671+21394C>T
|
|
|
ENST00000259455.3:c.1893+21394C>T
|
ENSP00000259455.2:n.1893+21394C>T
|
|
ENST00000634457.1:c.231+21394C>T
|
ENSP00000489352.1:n.231+21394C>T
|
|
ENST00000635462.1:n.388+21394C>T
|
|
|
NM_005458.7:c.1893+21394C>T
|
NP_005449.5:n.1893+21394C>T
|
|
XM_005252316.3:c.1119+21394C>T
|
XP_005252373.1:n.1119+21394C>T
|
|
XM_005252316.5:c.1119+21394C>T
|
XP_005252373.1:n.1119+21394C>T
|
|
XM_017015331.2:c.1599+21394C>T
|
XP_016870820.1:n.1599+21394C>T
|
|
XM_017015332.2:c.1119+21394C>T
|
XP_016870821.1:n.1119+21394C>T
|
|
NM_005458.8:c.1893+21394C>T
MANE Select
|
NP_005449.5:n.1893+21394C>T
|
|