ENST00000355697.7:c.818+229T>C
MANE Select
|
ENSP00000347924.2:n.818+229T>C
|
|
ENST00000355697.6:c.818+229T>C
|
ENSP00000347924.2:n.818+229T>C
|
|
ENST00000369131.8:c.470+229T>C
|
ENSP00000358127.4:n.470+229T>C
|
|
ENST00000461438.5:n.847+229T>C
|
|
|
ENST00000484960.5:n.148+229T>C
|
|
|
ENST00000490417.6:n.281+229T>C
|
|
|
NM_213649.1:c.818+229T>C
|
NP_998814.1:n.818+229T>C
|
|
NR_110305.1:n.836+229T>C
|
|
|
XM_005269525.3:c.791+229T>C
|
XP_005269582.1:n.791+229T>C
|
|
XM_005269526.1:c.470+229T>C
|
XP_005269583.1:n.470+229T>C
|
|
XM_005269527.1:c.470+229T>C
|
XP_005269584.1:n.470+229T>C
|
|
XM_011539282.1:c.470+229T>C
|
XP_011537584.1:n.470+229T>C
|
|
XR_945603.1:n.880+229T>C
|
|
|
XM_005269525.5:c.791+229T>C
|
XP_005269582.1:n.791+229T>C
|
|
XM_005269526.2:c.470+229T>C
|
XP_005269583.1:n.470+229T>C
|
|
XM_011539282.2:c.470+229T>C
|
XP_011537584.1:n.470+229T>C
|
|
XM_024447793.1:c.470+229T>C
|
XP_024303561.1:n.470+229T>C
|
|
XR_001747022.1:n.1069+229T>C
|
|
|
XR_001747023.1:n.963+229T>C
|
|
|
XR_945603.3:n.899+229T>C
|
|
|
NM_213649.2:c.818+229T>C
MANE Select
|
NP_998814.1:n.818+229T>C
|
|