ENST00000650060.2:c.996T>G
|
ENSP00000497272.1:p.His332Gln
|
|
ENST00000265986.11:c.996T>G
MANE Select
|
ENSP00000265986.6:p.His332Gln
|
|
ENST00000650060.1:c.996T>G
|
ENSP00000497272.1:p.His332Gln
|
|
ENST00000676540.1:c.996T>G
|
ENSP00000504633.1:p.His332Gln
|
|
ENST00000676626.1:n.1613T>G
|
|
|
ENST00000676816.1:c.996T>G
|
ENSP00000504709.1:p.His332Gln
|
|
ENST00000677079.1:c.996T>G
|
ENSP00000503417.1:p.His332Gln
|
|
ENST00000677096.1:c.*992T>G
|
ENSP00000503793.1:n.*992T>G
|
|
ENST00000677196.1:n.1073T>G
|
|
|
ENST00000677434.1:c.996T>G
|
ENSP00000503274.1:p.His332Gln
|
|
ENST00000677569.1:c.996T>G
|
ENSP00000503462.1:p.His332Gln
|
|
ENST00000677953.1:n.1073T>G
|
|
|
ENST00000677978.1:c.996T>G
|
ENSP00000503310.1:p.His332Gln
|
|
ENST00000678026.1:n.1613T>G
|
|
|
ENST00000678248.1:n.1073T>G
|
|
|
ENST00000678458.1:n.988T>G
|
|
|
ENST00000678673.1:c.996T>G
|
ENSP00000503082.1:p.His332Gln
|
|
ENST00000678715.1:c.873T>G
|
ENSP00000503025.1:p.His291Gln
|
|
ENST00000678844.1:c.996T>G
|
ENSP00000504561.1:p.His332Gln
|
|
ENST00000678977.1:n.1073T>G
|
|
|
ENST00000679069.1:n.1073T>G
|
|
|
ENST00000679089.1:c.996T>G
|
ENSP00000504067.1:p.His332Gln
|
|
ENST00000679174.1:c.996T>G
|
ENSP00000504758.1:p.His332Gln
|
|
ENST00000679222.1:c.996T>G
|
ENSP00000504070.1:p.His332Gln
|
|
ENST00000679232.1:c.996T>G
|
ENSP00000503818.1:p.His332Gln
|
|
ENST00000679312.1:c.996T>G
|
ENSP00000504442.1:p.His332Gln
|
|
ENST00000265986.10:c.996T>G
|
ENSP00000265986.6:p.His332Gln
|
|
ENST00000478361.6:c.*1206T>G
|
ENSP00000473506.1:n.*1206T>G
|
|
NM_004969.3:c.996T>G
|
NP_004960.2:p.His332Gln
|
|
XM_005269766.2:c.996T>G
|
XP_005269823.1:p.His332Gln
|
|
XM_005269769.3:c.996T>G
|
XP_005269826.1:p.His332Gln
|
|
XR_945727.1:n.1070T>G
|
|
|
NM_001322793.1:c.996T>G
|
NP_001309722.1:p.His332Gln
|
|
NM_001322794.1:c.879T>G
|
NP_001309723.1:p.His293Gln
|
|
NM_001322795.1:c.873T>G
|
NP_001309724.1:p.His291Gln
|
|
NM_001322796.1:c.873T>G
|
NP_001309725.1:p.His291Gln
|
|
NR_136399.1:n.1072T>G
|
|
|
XM_017016187.1:c.873T>G
|
XP_016871676.1:p.His291Gln
|
|
XM_017016188.1:c.873T>G
|
XP_016871677.1:p.His291Gln
|
|
XM_017016189.1:c.873T>G
|
XP_016871678.1:p.His291Gln
|
|
XM_017016190.1:c.873T>G
|
XP_016871679.1:p.His291Gln
|
|
XR_001747103.2:n.1070T>G
|
|
|
XR_945727.3:n.1070T>G
|
|
|
NM_004969.4:c.996T>G
MANE Select
|
NP_004960.2:p.His332Gln
|
|
NM_001322793.2:c.996T>G
|
NP_001309722.1:p.His332Gln
|
|
NM_001322794.2:c.879T>G
|
NP_001309723.1:p.His293Gln
|
|
NM_001322795.2:c.873T>G
|
NP_001309724.1:p.His291Gln
|
|
NR_136399.2:n.1070T>G
|
|
|