|
ENST00000321169.10:c.-33G>C
(HACL1)
MANE Select
|
ENSP00000323811.5:n.-33G>C
|
|
|
ENST00000427382.2:c.-168C>G
(BTD)
|
ENSP00000397113.2:n.-168C>G
|
|
|
ENST00000449107.7:c.-291C>G
(BTD)
|
ENSP00000388212.2:n.-291C>G
|
|
|
ENST00000321169.9:c.-33G>C
(HACL1)
|
ENSP00000323811.5:n.-33G>C
|
|
|
ENST00000383779.8:c.-33G>C
(HACL1)
|
ENSP00000373289.4:n.-33G>C
|
|
|
ENST00000414979.1:c.-33G>C
(HACL1)
|
ENSP00000395352.1:n.-33G>C
|
|
|
ENST00000417015.1:c.92C>G
(BTD)
|
ENSP00000403775.1:p.Ala31Gly
|
|
|
ENST00000421993.5:c.-33G>C
(HACL1)
|
ENSP00000391393.1:n.-33G>C
|
|
|
ENST00000422591.5:c.-33G>C
(HACL1)
|
ENSP00000392796.1:n.-33G>C
|
|
|
ENST00000427382.1:c.-168C>G
(BTD)
|
ENSP00000397113.1:n.-168C>G
|
|
|
ENST00000435217.6:c.-33G>C
(HACL1)
|
ENSP00000395278.2:n.-33G>C
|
|
|
ENST00000451445.6:c.-33G>C
(HACL1)
|
ENSP00000403656.2:n.-33G>C
|
|
|
ENST00000456194.6:c.-33G>C
(HACL1)
|
ENSP00000390699.2:n.-33G>C
|
|
|
ENST00000457447.6:c.-33G>C
(HACL1)
|
ENSP00000404883.2:n.-33G>C
|
|
|
ENST00000460907.1:n.74G>C
(HACL1)
|
|
|
|
ENST00000472857.1:n.51G>C
(HACL1)
|
|
|
|
ENST00000494021.1:n.127C>G
(BTD)
|
|
|
|
ENST00000628377.2:c.-33G>C
(HACL1)
|
ENSP00000486684.1:n.-33G>C
|
|
|
NM_001281723.1:c.-225C>G
(BTD)
|
NP_001268652.1:n.-225C>G
|
|
|
NM_001284413.1:c.-33G>C
(HACL1)
|
NP_001271342.1:n.-33G>C
|
|
|
NM_001284415.1:c.-33G>C
(HACL1)
|
NP_001271344.1:n.-33G>C
|
|
|
NM_001284416.1:c.-33G>C
(HACL1)
|
NP_001271345.1:n.-33G>C
|
|
|
NM_012260.3:c.-33G>C
(HACL1)
|
NP_036392.2:n.-33G>C
|
|
|
NR_104315.1:n.357G>C
(HACL1)
|
|
|
|
NM_001281723.2:c.-225C>G
(BTD)
|
NP_001268652.1:n.-225C>G
|
|
|
NM_001281723.3:c.-291C>G
(BTD)
|
NP_001268652.2:n.-291C>G
|
|
|
NM_001284413.2:c.-33G>C
(HACL1)
|
NP_001271342.1:n.-33G>C
|
|
|
NM_001284415.2:c.-33G>C
(HACL1)
|
NP_001271344.1:n.-33G>C
|
|
|
NM_001284416.2:c.-33G>C
(HACL1)
|
NP_001271345.1:n.-33G>C
|
|
|
NM_012260.4:c.-33G>C
(HACL1)
MANE Select
|
NP_036392.2:n.-33G>C
|
|
|
NR_104315.2:n.74G>C
(HACL1)
|
|
|
