ENST00000272321.12:c.15T>G
MANE Select
|
ENSP00000272321.7:p.Phe5Leu
|
|
ENST00000272321.11:c.15T>G
|
ENSP00000272321.7:p.Phe5Leu
|
|
ENST00000409562.7:c.15T>G
|
ENSP00000387222.3:p.Phe5Leu
|
|
ENST00000409835.5:n.262T>G
|
|
|
ENST00000417238.5:c.15T>G
|
ENSP00000411429.1:p.Phe5Leu
|
|
ENST00000418148.5:c.10T>G
|
|
|
ENST00000431065.1:c.15T>G
|
ENSP00000396226.1:p.Phe5Leu
|
|
ENST00000467687.1:n.488+62402T>G
|
|
|
ENST00000484073.1:n.244T>G
|
|
|
ENST00000490935.5:n.583+62402T>G
|
|
|
NM_015910.5:c.15T>G
|
NP_056994.3:p.Phe5Leu
|
|
XM_005264348.2:c.15T>G
|
XP_005264405.1:p.Phe5Leu
|
|
XM_011532881.1:c.-310T>G
|
XP_011531183.1:n.-310T>G
|
|
XM_011532882.1:c.-25+62402T>G
|
XP_011531184.1:n.-25+62402T>G
|
|
XM_011532883.1:c.15T>G
|
XP_011531185.1:p.Phe5Leu
|
|
XM_011532884.1:c.15T>G
|
XP_011531186.1:p.Phe5Leu
|
|
XM_011532885.1:c.15T>G
|
XP_011531187.1:p.Phe5Leu
|
|
XM_011532886.1:c.15T>G
|
XP_011531188.1:p.Phe5Leu
|
|
XM_011532887.1:c.15T>G
|
XP_011531189.1:p.Phe5Leu
|
|
XM_011532888.1:c.15T>G
|
XP_011531190.1:p.Phe5Leu
|
|
XM_011532889.1:c.15T>G
|
XP_011531191.1:p.Phe5Leu
|
|
XM_011532890.1:c.15T>G
|
XP_011531192.1:p.Phe5Leu
|
|
XM_011532891.1:c.-310T>G
|
XP_011531193.1:n.-310T>G
|
|
XR_244934.1:n.262T>G
|
|
|
XR_244935.1:n.262T>G
|
|
|
XR_939686.1:n.262T>G
|
|
|
NM_001354044.1:c.-310T>G
|
NP_001340973.1:n.-310T>G
|
|
NM_001354045.1:c.15T>G
|
NP_001340974.1:p.Phe5Leu
|
|
NM_015910.6:c.15T>G
|
NP_056994.3:p.Phe5Leu
|
|
NR_148704.1:n.543T>G
|
|
|
NR_148705.1:n.543T>G
|
|
|
XM_005264348.4:c.15T>G
|
XP_005264405.1:p.Phe5Leu
|
|
XM_011532881.3:c.-310T>G
|
XP_011531183.1:n.-310T>G
|
|
XM_011532884.3:c.15T>G
|
XP_011531186.1:p.Phe5Leu
|
|
XM_011532887.3:c.15T>G
|
XP_011531189.1:p.Phe5Leu
|
|
XM_011532890.3:c.15T>G
|
XP_011531192.1:p.Phe5Leu
|
|
XM_011532891.2:c.-310T>G
|
XP_011531193.1:n.-310T>G
|
|
XM_017004253.2:c.15T>G
|
XP_016859742.1:p.Phe5Leu
|
|
XM_017004254.2:c.15T>G
|
XP_016859743.1:p.Phe5Leu
|
|
XR_001738759.2:n.477T>G
|
|
|
XR_001738760.2:n.477T>G
|
|
|
XR_002959303.1:n.477T>G
|
|
|
XR_244934.3:n.477T>G
|
|
|
NM_015910.7:c.15T>G
MANE Select
|
NP_056994.3:p.Phe5Leu
|
|
NM_001354044.2:c.-310T>G
|
NP_001340973.1:n.-310T>G
|
|
NM_001354045.2:c.15T>G
|
NP_001340974.1:p.Phe5Leu
|
|
NR_148704.2:n.221T>G
|
|
|
NR_148705.2:n.221T>G
|
|
|