|
ENST00000304494.10:c.167G>T
MANE Select
|
ENSP00000307101.5:p.Ser56Ile
|
|
|
ENST00000404796.3:c.348-58241C>A
|
ENSP00000385916.2:n.348-58241C>A
|
|
|
ENST00000579755.2:c.210G>T
MANE Plus Clinical
|
ENSP00000462950.1:p.Gln70His
|
|
|
ENST00000304494.9:c.167G>T
|
ENSP00000307101.5:p.Ser56Ile
|
|
|
ENST00000361570.4:c.210G>T
|
ENSP00000355153.4:p.Gln70His
|
|
|
ENST00000380150.2:n.141G>T
|
|
|
|
ENST00000380151.3:c.441G>T
|
ENSP00000369496.3:n.441G>T
|
|
|
ENST00000404796.2:c.348-58241C>A
|
ENSP00000385916.2:n.348-58241C>A
|
|
|
ENST00000479692.2:c.14G>T
|
ENSP00000466887.1:p.Ser5Ile
|
|
|
ENST00000494262.5:c.14G>T
|
ENSP00000464952.1:p.Ser5Ile
|
|
|
ENST00000497750.1:c.14G>T
|
ENSP00000468510.1:p.Ser5Ile
|
|
|
ENST00000498124.1:c.167G>T
|
ENSP00000418915.1:p.Ser56Ile
|
|
|
ENST00000498628.6:c.14G>T
|
ENSP00000467857.1:p.Ser5Ile
|
|
|
ENST00000530628.2:c.210G>T
|
ENSP00000432664.2:p.Gln70His
|
|
|
ENST00000578845.2:c.14G>T
|
ENSP00000467390.1:p.Ser5Ile
|
|
|
ENST00000579122.1:c.167G>T
|
ENSP00000464202.1:p.Ser56Ile
|
|
|
ENST00000579755.1:c.210G>T
|
ENSP00000462950.1:p.Gln70His
|
|
|
NM_000077.4:c.167G>T , LRG_11t1:c.167G>T
|
NP_000068.1:p.Ser56Ile
|
|
|
NM_001195132.1:c.167G>T
|
NP_001182061.1:p.Ser56Ile
|
|
|
NM_058195.3:c.210G>T , LRG_11t2:c.210G>T
|
NP_478102.2:p.Gln70His
|
|
|
NM_058197.4:c.441G>T
|
NP_478104.2:n.441G>T
|
|
|
XM_005251343.1:c.14G>T
|
XP_005251400.1:p.Ser5Ile
|
|
|
XM_011517675.1:c.167G>T
|
XP_011515977.1:p.Ser56Ile
|
|
|
XM_011517676.1:c.167G>T
|
XP_011515978.1:p.Ser56Ile
|
|
|
XM_011517679.1:c.14G>T
|
XP_011515981.1:p.Ser5Ile
|
|
|
XR_929159.1:n.568G>T
|
|
|
|
XR_929161.1:n.357G>T
|
|
|
|
XR_929162.1:n.357G>T
|
|
|
|
XR_929163.1:n.306G>T
|
|
|
|
XR_929164.1:n.89G>T
|
|
|
|
NM_001363763.1:c.14G>T
|
NP_001350692.1:p.Ser5Ile
|
|
|
XM_011517675.2:c.167G>T
|
XP_011515977.1:p.Ser56Ile
|
|
|
XM_011517676.2:c.167G>T
|
XP_011515978.1:p.Ser56Ile
|
|
|
XR_929159.2:n.497G>T
|
|
|
|
NM_001363763.2:c.14G>T
|
NP_001350692.1:p.Ser5Ile
|
|
|
NM_000077.5:c.167G>T
MANE Select
|
NP_000068.1:p.Ser56Ile
|
|
|
NM_001195132.2:c.167G>T
|
NP_001182061.1:p.Ser56Ile
|
|
|
NM_058195.4:c.210G>T
MANE Plus Clinical
|
NP_478102.2:p.Gln70His
|
|
|
NM_058197.5:c.*90G>T
|
NP_478104.2:n.*90G>T
|
|
