ENST00000323274.15:c.833A>G
(TYMS)
MANE Select
|
ENSP00000315644.10:p.Lys278Arg
|
|
ENST00000647584.2:c.*1417T>C
(ENOSF1)
MANE Select
|
ENSP00000497230.2:n.*1417T>C
|
|
ENST00000323224.7:c.731A>G
(TYMS)
|
ENSP00000314727.7:p.Lys244Arg
|
|
ENST00000323250.9:c.584A>G
(TYMS)
|
ENSP00000314902.5:p.Lys195Arg
|
|
ENST00000323274.14:c.833A>G
(TYMS)
|
ENSP00000315644.10:p.Lys278Arg
|
|
ENST00000383578.7:c.*333T>C
(ENOSF1)
|
ENSP00000373072.3:n.*333T>C
|
|
ENST00000581920.1:n.411A>G
(TYMS)
|
|
|
ENST00000584259.6:n.3776T>C
(ENOSF1)
|
|
|
NM_001071.2:c.833A>G , LRG_783t1:c.833A>G
(TYMS)
|
NP_001062.1:p.Lys278Arg
|
|
NM_001126123.3:c.*333T>C
(ENOSF1)
|
NP_001119595.1:n.*333T>C
|
|
NM_017512.5:c.*1417T>C
(ENOSF1)
|
NP_059982.2:n.*1417T>C
|
|
NM_202758.3:c.*1417T>C
(ENOSF1)
|
NP_974487.1:n.*1417T>C
|
|
XR_243810.3:n.1701T>C
(ENOSF1)
|
|
|
XR_243811.2:n.1726T>C
(ENOSF1)
|
|
|
XR_430041.2:n.1821T>C
(ENOSF1)
|
|
|
NM_001071.3:c.833A>G
(TYMS)
|
NP_001062.1:p.Lys278Arg
|
|
NM_001354867.1:c.731A>G
(TYMS)
|
NP_001341796.1:p.Lys244Arg
|
|
NM_001354868.1:c.584A>G
(TYMS)
|
NP_001341797.1:p.Lys195Arg
|
|
NR_148706.1:n.1626T>C
(ENOSF1)
|
|
|
NR_148707.1:n.1742T>C
(ENOSF1)
|
|
|
NR_148708.1:n.1990T>C
(ENOSF1)
|
|
|
NR_148709.1:n.1676T>C
(ENOSF1)
|
|
|
NR_148710.1:n.1702T>C
(ENOSF1)
|
|
|
NR_148711.1:n.1553T>C
(ENOSF1)
|
|
|
NR_148712.1:n.1886T>C
(ENOSF1)
|
|
|
XM_024451242.1:c.452A>G
(TYMS)
|
XP_024307010.1:p.Lys151Arg
|
|
XR_002958180.1:n.1454T>C
(ENOSF1)
|
|
|
XR_430041.4:n.1840T>C
(ENOSF1)
|
|
|
NM_001071.4:c.833A>G
(TYMS)
MANE Select
|
NP_001062.1:p.Lys278Arg
|
|
NM_017512.7:c.*1417T>C
(ENOSF1)
MANE Select
|
NP_059982.2:n.*1417T>C
|
|
NM_001318760.2:c.*1417T>C
(ENOSF1)
|
NP_001305689.1:n.*1417T>C
|
|
NM_001354065.2:c.*1417T>C
(ENOSF1)
|
NP_001340994.1:n.*1417T>C
|
|
NM_001354066.2:c.*1417T>C
(ENOSF1)
|
NP_001340995.1:n.*1417T>C
|
|
NM_001354067.2:c.*1417T>C
(ENOSF1)
|
NP_001340996.1:n.*1417T>C
|
|
NM_001354068.2:c.*1417T>C
(ENOSF1)
|
NP_001340997.1:n.*1417T>C
|
|
NM_001354867.2:c.731A>G
(TYMS)
|
NP_001341796.1:p.Lys244Arg
|
|
NM_001354868.2:c.584A>G
(TYMS)
|
NP_001341797.1:p.Lys195Arg
|
|
NM_202758.5:c.*1417T>C
(ENOSF1)
|
NP_974487.2:n.*1417T>C
|
|
NR_148706.2:n.1592T>C
(ENOSF1)
|
|
|
NR_148707.2:n.1708T>C
(ENOSF1)
|
|
|
NR_148708.2:n.1956T>C
(ENOSF1)
|
|
|
NR_148709.2:n.1642T>C
(ENOSF1)
|
|
|
NR_148710.2:n.1668T>C
(ENOSF1)
|
|
|
NR_148711.2:n.1519T>C
(ENOSF1)
|
|
|
NR_148712.2:n.1852T>C
(ENOSF1)
|
|
|