ENST00000379644.9:c.821-411C>T
MANE Select
|
ENSP00000368965.4:n.821-411C>T
|
|
ENST00000379644.8:c.821-411C>T
|
ENSP00000368965.4:n.821-411C>T
|
|
ENST00000520704.1:c.*270-411C>T
|
ENSP00000429109.1:n.*270-411C>T
|
|
ENST00000522082.5:c.62-411C>T
|
ENSP00000430151.1:n.62-411C>T
|
|
NM_152419.2:c.821-411C>T
|
NP_689632.2:n.821-411C>T
|
|
XM_005273409.1:c.821-411C>T
|
XP_005273466.1:n.821-411C>T
|
|
XM_005273410.1:c.821-411C>T
|
XP_005273467.1:n.821-411C>T
|
|
XM_005273411.1:c.820+916C>T
|
XP_005273468.1:n.820+916C>T
|
|
XM_005273412.2:c.821-411C>T
|
XP_005273469.1:n.821-411C>T
|
|
NM_001363227.1:c.821-411C>T
|
NP_001350156.1:n.821-411C>T
|
|
NM_001363228.1:c.820+916C>T
|
NP_001350157.1:n.820+916C>T
|
|
NM_001363229.1:c.-14+916C>T
|
NP_001350158.1:n.-14+916C>T
|
|
XM_005273412.4:c.821-411C>T
|
XP_005273469.1:n.821-411C>T
|
|
NM_152419.3:c.821-411C>T
MANE Select
|
NP_689632.2:n.821-411C>T
|
|
NM_001363227.2:c.821-411C>T
|
NP_001350156.1:n.821-411C>T
|
|
NM_001363228.2:c.820+916C>T
|
NP_001350157.1:n.820+916C>T
|
|
NM_001363229.2:c.-14+916C>T
|
NP_001350158.1:n.-14+916C>T
|
|