ENST00000376486.3:c.-11+207A>C
|
ENSP00000365669.3:n.-11+207A>C
|
|
ENST00000376590.9:c.-14+207A>C
MANE Select
|
ENSP00000365775.3:n.-14+207A>C
|
|
ENST00000641437.1:n.119+207A>C
|
|
|
ENST00000641446.1:c.-14+207A>C
|
ENSP00000493262.1:n.-14+207A>C
|
|
ENST00000641747.1:c.-14+207A>C
|
ENSP00000493116.1:n.-14+207A>C
|
|
ENST00000642002.1:n.216+207A>C
|
|
|
ENST00000376486.2:c.-14+207A>C
|
ENSP00000365669.2:n.-14+207A>C
|
|
ENST00000376590.7:c.-14+207A>C
|
ENSP00000365775.3:n.-14+207A>C
|
|
ENST00000418034.1:c.-348A>C
|
ENSP00000405082.1:n.-348A>C
|
|
NM_005957.4:c.-14+207A>C , LRG_726t1:c.-14+207A>C
|
NP_005948.3:n.-14+207A>C
|
|
XM_005263460.3:c.-348A>C
|
XP_005263517.1:n.-348A>C
|
|
XM_005263461.3:c.-345A>C
|
XP_005263518.1:n.-345A>C
|
|
XM_005263462.3:c.-11+207A>C
|
XP_005263519.1:n.-11+207A>C
|
|
XM_005263463.2:c.-277+207A>C
|
XP_005263520.1:n.-277+207A>C
|
|
XM_005263460.5:c.-348A>C
|
XP_005263517.1:n.-348A>C
|
|
XM_005263462.4:c.-11+207A>C
|
XP_005263519.1:n.-11+207A>C
|
|
XM_005263463.4:c.-277+207A>C
|
XP_005263520.1:n.-277+207A>C
|
|
NM_005957.5:c.-14+207A>C
MANE Select
|
NP_005948.3:n.-14+207A>C
|
|