ENST00000323274.15:c.838A>G
(TYMS)
MANE Select
|
ENSP00000315644.10:p.Arg280Gly
|
|
ENST00000647584.2:c.*1412T>C
(ENOSF1)
MANE Select
|
ENSP00000497230.2:n.*1412T>C
|
|
ENST00000323224.7:c.736A>G
(TYMS)
|
ENSP00000314727.7:p.Arg246Gly
|
|
ENST00000323250.9:c.589A>G
(TYMS)
|
ENSP00000314902.5:p.Arg197Gly
|
|
ENST00000323274.14:c.838A>G
(TYMS)
|
ENSP00000315644.10:p.Arg280Gly
|
|
ENST00000383578.7:c.*328T>C
(ENOSF1)
|
ENSP00000373072.3:n.*328T>C
|
|
ENST00000581920.1:n.416A>G
(TYMS)
|
|
|
ENST00000584259.6:n.3771T>C
(ENOSF1)
|
|
|
NM_001071.2:c.838A>G , LRG_783t1:c.838A>G
(TYMS)
|
NP_001062.1:p.Arg280Gly
|
|
NM_001126123.3:c.*328T>C
(ENOSF1)
|
NP_001119595.1:n.*328T>C
|
|
NM_017512.5:c.*1412T>C
(ENOSF1)
|
NP_059982.2:n.*1412T>C
|
|
NM_202758.3:c.*1412T>C
(ENOSF1)
|
NP_974487.1:n.*1412T>C
|
|
XR_243810.3:n.1696T>C
(ENOSF1)
|
|
|
XR_243811.2:n.1721T>C
(ENOSF1)
|
|
|
XR_430041.2:n.1816T>C
(ENOSF1)
|
|
|
NM_001071.3:c.838A>G
(TYMS)
|
NP_001062.1:p.Arg280Gly
|
|
NM_001354867.1:c.736A>G
(TYMS)
|
NP_001341796.1:p.Arg246Gly
|
|
NM_001354868.1:c.589A>G
(TYMS)
|
NP_001341797.1:p.Arg197Gly
|
|
NR_148706.1:n.1621T>C
(ENOSF1)
|
|
|
NR_148707.1:n.1737T>C
(ENOSF1)
|
|
|
NR_148708.1:n.1985T>C
(ENOSF1)
|
|
|
NR_148709.1:n.1671T>C
(ENOSF1)
|
|
|
NR_148710.1:n.1697T>C
(ENOSF1)
|
|
|
NR_148711.1:n.1548T>C
(ENOSF1)
|
|
|
NR_148712.1:n.1881T>C
(ENOSF1)
|
|
|
XM_024451242.1:c.457A>G
(TYMS)
|
XP_024307010.1:p.Arg153Gly
|
|
XR_002958180.1:n.1449T>C
(ENOSF1)
|
|
|
XR_430041.4:n.1835T>C
(ENOSF1)
|
|
|
NM_001071.4:c.838A>G
(TYMS)
MANE Select
|
NP_001062.1:p.Arg280Gly
|
|
NM_017512.7:c.*1412T>C
(ENOSF1)
MANE Select
|
NP_059982.2:n.*1412T>C
|
|
NM_001318760.2:c.*1412T>C
(ENOSF1)
|
NP_001305689.1:n.*1412T>C
|
|
NM_001354065.2:c.*1412T>C
(ENOSF1)
|
NP_001340994.1:n.*1412T>C
|
|
NM_001354066.2:c.*1412T>C
(ENOSF1)
|
NP_001340995.1:n.*1412T>C
|
|
NM_001354067.2:c.*1412T>C
(ENOSF1)
|
NP_001340996.1:n.*1412T>C
|
|
NM_001354068.2:c.*1412T>C
(ENOSF1)
|
NP_001340997.1:n.*1412T>C
|
|
NM_001354867.2:c.736A>G
(TYMS)
|
NP_001341796.1:p.Arg246Gly
|
|
NM_001354868.2:c.589A>G
(TYMS)
|
NP_001341797.1:p.Arg197Gly
|
|
NM_202758.5:c.*1412T>C
(ENOSF1)
|
NP_974487.2:n.*1412T>C
|
|
NR_148706.2:n.1587T>C
(ENOSF1)
|
|
|
NR_148707.2:n.1703T>C
(ENOSF1)
|
|
|
NR_148708.2:n.1951T>C
(ENOSF1)
|
|
|
NR_148709.2:n.1637T>C
(ENOSF1)
|
|
|
NR_148710.2:n.1663T>C
(ENOSF1)
|
|
|
NR_148711.2:n.1514T>C
(ENOSF1)
|
|
|
NR_148712.2:n.1847T>C
(ENOSF1)
|
|
|