ENST00000323274.15:c.805-482A>G
(TYMS)
MANE Select
|
ENSP00000315644.10:n.805-482A>G
|
|
ENST00000647584.2:c.*1927T>C
(ENOSF1)
MANE Select
|
ENSP00000497230.2:n.*1927T>C
|
|
ENST00000323224.7:c.703-482A>G
(TYMS)
|
ENSP00000314727.7:n.703-482A>G
|
|
ENST00000323250.9:c.556-482A>G
(TYMS)
|
ENSP00000314902.5:n.556-482A>G
|
|
ENST00000323274.14:c.805-482A>G
(TYMS)
|
ENSP00000315644.10:n.805-482A>G
|
|
ENST00000383578.7:c.*843T>C
(ENOSF1)
|
ENSP00000373072.3:n.*843T>C
|
|
ENST00000581920.1:n.383-482A>G
(TYMS)
|
|
|
ENST00000584259.6:n.4286T>C
(ENOSF1)
|
|
|
NM_001071.2:c.805-482A>G , LRG_783t1:c.805-482A>G
(TYMS)
|
NP_001062.1:n.805-482A>G
|
|
NM_001126123.3:c.*843T>C
(ENOSF1)
|
NP_001119595.1:n.*843T>C
|
|
NM_017512.5:c.*1927T>C
(ENOSF1)
|
NP_059982.2:n.*1927T>C
|
|
NM_202758.3:c.*1927T>C
(ENOSF1)
|
NP_974487.1:n.*1927T>C
|
|
NM_001071.3:c.805-482A>G
(TYMS)
|
NP_001062.1:n.805-482A>G
|
|
NM_001354867.1:c.703-482A>G
(TYMS)
|
NP_001341796.1:n.703-482A>G
|
|
NM_001354868.1:c.556-482A>G
(TYMS)
|
NP_001341797.1:n.556-482A>G
|
|
NR_148706.1:n.2136T>C
(ENOSF1)
|
|
|
NR_148707.1:n.2252T>C
(ENOSF1)
|
|
|
NR_148708.1:n.2500T>C
(ENOSF1)
|
|
|
NR_148709.1:n.2186T>C
(ENOSF1)
|
|
|
NR_148710.1:n.2212T>C
(ENOSF1)
|
|
|
NR_148711.1:n.2063T>C
(ENOSF1)
|
|
|
NR_148712.1:n.2396T>C
(ENOSF1)
|
|
|
XM_024451242.1:c.424-482A>G
(TYMS)
|
XP_024307010.1:n.424-482A>G
|
|
XR_002958180.1:n.1964T>C
(ENOSF1)
|
|
|
XR_430041.4:n.2350T>C
(ENOSF1)
|
|
|
NM_001071.4:c.805-482A>G
(TYMS)
MANE Select
|
NP_001062.1:n.805-482A>G
|
|
NM_017512.7:c.*1927T>C
(ENOSF1)
MANE Select
|
NP_059982.2:n.*1927T>C
|
|
NM_001318760.2:c.*1927T>C
(ENOSF1)
|
NP_001305689.1:n.*1927T>C
|
|
NM_001354065.2:c.*1927T>C
(ENOSF1)
|
NP_001340994.1:n.*1927T>C
|
|
NM_001354066.2:c.*1927T>C
(ENOSF1)
|
NP_001340995.1:n.*1927T>C
|
|
NM_001354067.2:c.*1927T>C
(ENOSF1)
|
NP_001340996.1:n.*1927T>C
|
|
NM_001354068.2:c.*1927T>C
(ENOSF1)
|
NP_001340997.1:n.*1927T>C
|
|
NM_001354867.2:c.703-482A>G
(TYMS)
|
NP_001341796.1:n.703-482A>G
|
|
NM_001354868.2:c.556-482A>G
(TYMS)
|
NP_001341797.1:n.556-482A>G
|
|
NM_202758.5:c.*1927T>C
(ENOSF1)
|
NP_974487.2:n.*1927T>C
|
|
NR_148706.2:n.2102T>C
(ENOSF1)
|
|
|
NR_148707.2:n.2218T>C
(ENOSF1)
|
|
|
NR_148708.2:n.2466T>C
(ENOSF1)
|
|
|
NR_148709.2:n.2152T>C
(ENOSF1)
|
|
|
NR_148710.2:n.2178T>C
(ENOSF1)
|
|
|
NR_148711.2:n.2029T>C
(ENOSF1)
|
|
|
NR_148712.2:n.2362T>C
(ENOSF1)
|
|
|