|
ENST00000397990.5:c.173G>A
(ANG)
MANE Select
|
ENSP00000381077.4:p.Gly58Asp
|
|
|
ENST00000555835.3:c.-17-5618G>A
(RNASE4)
MANE Select
|
ENSP00000452245.1:n.-17-5618G>A
|
|
|
ENST00000336811.10:c.173G>A
(ANG)
|
ENSP00000336762.6:p.Gly58Asp
|
|
|
ENST00000397990.4:c.173G>A
(ANG)
|
ENSP00000381077.4:p.Gly58Asp
|
|
|
ENST00000397995.2:c.-17-5618G>A
(RNASE4)
|
ENSP00000381081.2:n.-17-5618G>A
|
|
|
ENST00000553909.1:c.86+87G>A
|
ENSP00000477037.1:n.86+87G>A
|
|
|
ENST00000554073.1:n.146-5129G>A
(ANG)
|
|
|
|
ENST00000555597.1:c.-18+4863G>A
(RNASE4)
|
ENSP00000451624.1:n.-18+4863G>A
|
|
|
ENST00000555835.2:c.-17-5618G>A
(RNASE4)
|
ENSP00000452245.1:n.-17-5618G>A
|
|
|
NM_001097577.2:c.173G>A
(ANG)
|
NP_001091046.1:p.Gly58Asp
|
|
|
NM_001145.4:c.173G>A , LRG_653t1:c.173G>A
(ANG)
|
NP_001136.1:p.Gly58Asp
|
|
|
NM_001282192.1:c.-18+87G>A
(RNASE4)
|
NP_001269121.1:n.-18+87G>A
|
|
|
NM_001282193.1:c.-17-5618G>A
(RNASE4)
|
NP_001269122.1:n.-17-5618G>A
|
|
|
NM_002937.4:c.-17-5618G>A
(RNASE4)
|
NP_002928.1:n.-17-5618G>A
|
|
|
NM_194431.2:c.-18+4863G>A
(RNASE4)
|
NP_919412.1:n.-18+4863G>A
|
|
|
NM_002937.5:c.-17-5618G>A
(RNASE4)
MANE Select
|
NP_002928.1:n.-17-5618G>A
|
|
|
NM_001097577.3:c.173G>A
(ANG)
MANE Select
|
NP_001091046.1:p.Gly58Asp
|
|
|
NM_001282192.2:c.-18+87G>A
(RNASE4)
|
NP_001269121.1:n.-18+87G>A
|
|
|
NM_001282193.2:c.-17-5618G>A
(RNASE4)
|
NP_001269122.1:n.-17-5618G>A
|
|
|
NM_194431.3:c.-18+4863G>A
(RNASE4)
|
NP_919412.1:n.-18+4863G>A
|
|
|
NM_001385271.1:c.173G>A
(ANG)
|
NP_001372200.1:p.Gly58Asp
|
|
|
NM_001385272.1:c.173G>A
(ANG)
|
NP_001372201.1:p.Gly58Asp
|
|
|
NM_001385273.1:c.173G>A
(ANG)
|
NP_001372202.1:p.Gly58Asp
|
|
|
NM_001385274.1:c.173G>A
(ANG)
|
NP_001372203.1:p.Gly58Asp
|
|
|
NR_174964.1:n.479C>T
(EGILA)
|
|
|
