|
ENST00000507079.6:c.860-193G>T
|
ENSP00000426147.2:n.860-193G>T
|
|
|
ENST00000509165.2:c.836-193G>T
|
ENSP00000423877.2:n.836-193G>T
|
|
|
ENST00000697794.1:c.*477-193G>T
|
ENSP00000513443.1:n.*477-193G>T
|
|
|
ENST00000697799.1:n.333-193G>T
|
|
|
|
ENST00000697800.1:n.47-193G>T
|
|
|
|
ENST00000226574.9:c.836-193G>T
MANE Select
|
ENSP00000226574.4:n.836-193G>T
|
|
|
ENST00000652569.1:c.811+39G>T
|
|
|
|
ENST00000652619.1:c.857-193G>T
|
ENSP00000499031.1:n.857-193G>T
|
|
|
ENST00000226574.8:c.836-193G>T
|
ENSP00000226574.4:n.836-193G>T
|
|
|
ENST00000394820.8:c.833-193G>T
|
ENSP00000378297.4:n.833-193G>T
|
|
|
ENST00000505458.5:c.833-193G>T
|
ENSP00000424790.1:n.833-193G>T
|
|
|
ENST00000508584.1:c.215-193G>T
|
ENSP00000424815.1:n.215-193G>T
|
|
|
ENST00000600343.5:c.293-193G>T
|
ENSP00000469340.1:n.293-193G>T
|
|
|
NM_001165412.1:c.833-193G>T
|
NP_001158884.1:n.833-193G>T
|
|
|
NM_003998.3:c.836-193G>T
|
NP_003989.2:n.836-193G>T
|
|
|
XM_011532006.1:c.857-193G>T
|
XP_011530308.1:n.857-193G>T
|
|
|
XM_011532007.1:c.833-193G>T
|
XP_011530309.1:n.833-193G>T
|
|
|
XM_011532008.1:c.677-193G>T
|
XP_011530310.1:n.677-193G>T
|
|
|
XM_011532009.1:c.440-193G>T
|
XP_011530311.1:n.440-193G>T
|
|
|
NM_001319226.1:c.833-193G>T
|
NP_001306155.1:n.833-193G>T
|
|
|
XM_011532006.2:c.857-193G>T
|
XP_011530308.1:n.857-193G>T
|
|
|
XM_024454067.1:c.860-193G>T
|
XP_024309835.1:n.860-193G>T
|
|
|
XM_024454068.1:c.836-193G>T
|
XP_024309836.1:n.836-193G>T
|
|
|
XM_024454069.1:c.701-193G>T
|
XP_024309837.1:n.701-193G>T
|
|
|
NM_003998.4:c.836-193G>T
MANE Select
|
NP_003989.2:n.836-193G>T
|
|
|
NM_001165412.2:c.833-193G>T
|
NP_001158884.1:n.833-193G>T
|
|
|
NM_001319226.2:c.833-193G>T
|
NP_001306155.1:n.833-193G>T
|
|
|
NM_001382625.1:c.836-193G>T
|
NP_001369554.1:n.836-193G>T
|
|
|
NM_001382626.1:c.836-193G>T
|
NP_001369555.1:n.836-193G>T
|
|
|
NM_001382627.1:c.833-193G>T
|
NP_001369556.1:n.833-193G>T
|
|
|
NM_001382628.1:c.794-193G>T
|
NP_001369557.1:n.794-193G>T
|
|
