ENST00000332955.7:c.235+131T>G
MANE Select
|
ENSP00000327786.2:n.235+131T>G
|
|
ENST00000332955.6:c.235+131T>G
|
ENSP00000327786.2:n.235+131T>G
|
|
ENST00000595517.5:c.168+198T>G
|
ENSP00000471815.1:n.168+198T>G
|
|
ENST00000595937.5:c.235+131T>G
|
ENSP00000470144.1:n.235+131T>G
|
|
ENST00000597553.1:n.687T>G
|
|
|
ENST00000602105.1:c.-104-206T>G
|
ENSP00000471134.1:n.-104-206T>G
|
|
NM_182575.2:c.235+131T>G
|
NP_872381.2:n.235+131T>G
|
|
XM_005258793.3:c.313+131T>G
|
XP_005258850.1:n.313+131T>G
|
|
XM_005258797.3:c.-104-206T>G
|
XP_005258854.1:n.-104-206T>G
|
|
XM_005258798.3:c.-104-206T>G
|
XP_005258855.1:n.-104-206T>G
|
|
XM_011526811.1:c.334+131T>G
|
XP_011525113.1:n.334+131T>G
|
|
XM_011526812.1:c.235+131T>G
|
XP_011525114.1:n.235+131T>G
|
|
XM_011526813.1:c.235+131T>G
|
XP_011525115.1:n.235+131T>G
|
|
XM_011526814.1:c.31T>G
|
XP_011525116.1:p.Phe11Val
|
|
XM_011526815.1:c.-113T>G
|
XP_011525117.1:n.-113T>G
|
|
XM_011526816.1:c.-104-206T>G
|
XP_011525118.1:n.-104-206T>G
|
|
XM_011526817.1:c.-104-206T>G
|
XP_011525119.1:n.-104-206T>G
|
|
XR_243923.2:n.1248+131T>G
|
|
|
XR_430196.2:n.1248+131T>G
|
|
|
XR_935799.1:n.1248+131T>G
|
|
|
NM_001321864.1:c.-104-206T>G
|
NP_001308793.1:n.-104-206T>G
|
|
NM_001321865.1:c.-325+131T>G
|
NP_001308794.1:n.-325+131T>G
|
|
NR_135832.1:n.241+198T>G
|
|
|
NM_182575.3:c.235+131T>G
MANE Select
|
NP_872381.2:n.235+131T>G
|
|