ENST00000529510.6:n.108G>T
|
|
|
ENST00000697846.1:n.108G>T
|
|
|
ENST00000697847.1:n.108G>T
|
|
|
ENST00000697848.1:n.108G>T
|
|
|
ENST00000697849.1:n.352G>T
|
|
|
ENST00000697850.1:n.108G>T
|
|
|
ENST00000697851.1:n.352G>T
|
|
|
ENST00000638186.1:n.182G>T
|
|
|
ENST00000638360.1:n.116G>T
|
|
|
ENST00000638925.1:n.115G>T
|
|
|
ENST00000650539.1:n.284G>T
|
|
|
ENST00000330775.9:c.-122G>T
|
ENSP00000476242.2:n.-122G>T
|
|
ENST00000357590.9:c.-122G>T
|
ENSP00000476176.2:n.-122G>T
|
|
ENST00000525039.5:n.302G>T
|
|
|
ENST00000525102.5:n.636G>T
|
|
|
ENST00000525787.1:n.174G>T
|
|
|
ENST00000526626.6:n.74G>T
|
|
|
ENST00000527992.5:n.106G>T
|
|
|
ENST00000530407.5:n.98G>T
|
|
|
ENST00000532085.1:n.1373G>T
|
|
|
ENST00000532888.6:n.74G>T
|
|
|
ENST00000534384.1:n.99G>T
|
|
|
ENST00000538950.5:c.-271G>T
|
ENSP00000475991.2:n.-271G>T
|
|
ENST00000545985.5:c.-122G>T
|
ENSP00000475241.2:n.-122G>T
|
|
NM_001164277.1:c.-122G>T , LRG_187t1:c.-122G>T
|
NP_001157749.1:n.-122G>T
|
|
NM_001164278.1:c.-122G>T
|
NP_001157750.1:n.-122G>T
|
|
NM_001164279.1:c.-271G>T
|
NP_001157751.1:n.-271G>T
|
|
NM_001164280.1:c.-122G>T
|
NP_001157752.1:n.-122G>T
|
|
NM_001467.5:c.-122G>T
|
NP_001458.1:n.-122G>T
|
|
NM_001164278.2:c.-122G>T
|
NP_001157750.1:n.-122G>T
|
|
NM_001164279.2:c.-271G>T
|
NP_001157751.1:n.-271G>T
|
|
NM_001467.6:c.-122G>T
|
NP_001458.1:n.-122G>T
|
|
NM_001164277.2:c.-122G>T
MANE Select
|
NP_001157749.1:n.-122G>T
|
|