ENST00000355697.7:c.471+1G>T
MANE Select
|
ENSP00000347924.2:n.471+1G>T
|
|
ENST00000355697.6:c.471+1G>T
|
ENSP00000347924.2:n.471+1G>T
|
|
ENST00000369131.8:c.123+1G>T
|
ENSP00000358127.4:n.123+1G>T
|
|
ENST00000419372.5:c.123+1G>T
|
ENSP00000414193.1:n.123+1G>T
|
|
ENST00000461438.5:n.500+1G>T
|
|
|
ENST00000466218.5:n.420+1G>T
|
|
|
NM_213649.1:c.471+1G>T
|
NP_998814.1:n.471+1G>T
|
|
NR_110305.1:n.489+1G>T
|
|
|
XM_005269525.3:c.444+1G>T
|
XP_005269582.1:n.444+1G>T
|
|
XM_005269526.1:c.123+1G>T
|
XP_005269583.1:n.123+1G>T
|
|
XM_005269527.1:c.123+1G>T
|
XP_005269584.1:n.123+1G>T
|
|
XM_011539282.1:c.123+1G>T
|
XP_011537584.1:n.123+1G>T
|
|
XR_945603.1:n.533+1G>T
|
|
|
XM_005269525.5:c.444+1G>T
|
XP_005269582.1:n.444+1G>T
|
|
XM_005269526.2:c.123+1G>T
|
XP_005269583.1:n.123+1G>T
|
|
XM_011539282.2:c.123+1G>T
|
XP_011537584.1:n.123+1G>T
|
|
XM_024447793.1:c.123+1G>T
|
XP_024303561.1:n.123+1G>T
|
|
XR_001747022.1:n.722+1G>T
|
|
|
XR_001747023.1:n.616+1G>T
|
|
|
XR_945603.3:n.552+1G>T
|
|
|
NM_213649.2:c.471+1G>T
MANE Select
|
NP_998814.1:n.471+1G>T
|
|