ENST00000323274.15:c.805-484G>A
(TYMS)
MANE Select
|
ENSP00000315644.10:n.805-484G>A
|
|
ENST00000647584.2:c.*1929C>T
(ENOSF1)
MANE Select
|
ENSP00000497230.2:n.*1929C>T
|
|
ENST00000323224.7:c.703-484G>A
(TYMS)
|
ENSP00000314727.7:n.703-484G>A
|
|
ENST00000323250.9:c.556-484G>A
(TYMS)
|
ENSP00000314902.5:n.556-484G>A
|
|
ENST00000323274.14:c.805-484G>A
(TYMS)
|
ENSP00000315644.10:n.805-484G>A
|
|
ENST00000383578.7:c.*845C>T
(ENOSF1)
|
ENSP00000373072.3:n.*845C>T
|
|
ENST00000581920.1:n.383-484G>A
(TYMS)
|
|
|
ENST00000584259.6:n.4288C>T
(ENOSF1)
|
|
|
NM_001071.2:c.805-484G>A , LRG_783t1:c.805-484G>A
(TYMS)
|
NP_001062.1:n.805-484G>A
|
|
NM_001126123.3:c.*845C>T
(ENOSF1)
|
NP_001119595.1:n.*845C>T
|
|
NM_017512.5:c.*1929C>T
(ENOSF1)
|
NP_059982.2:n.*1929C>T
|
|
NM_202758.3:c.*1929C>T
(ENOSF1)
|
NP_974487.1:n.*1929C>T
|
|
NM_001071.3:c.805-484G>A
(TYMS)
|
NP_001062.1:n.805-484G>A
|
|
NM_001354867.1:c.703-484G>A
(TYMS)
|
NP_001341796.1:n.703-484G>A
|
|
NM_001354868.1:c.556-484G>A
(TYMS)
|
NP_001341797.1:n.556-484G>A
|
|
NR_148706.1:n.2138C>T
(ENOSF1)
|
|
|
NR_148707.1:n.2254C>T
(ENOSF1)
|
|
|
NR_148708.1:n.2502C>T
(ENOSF1)
|
|
|
NR_148709.1:n.2188C>T
(ENOSF1)
|
|
|
NR_148710.1:n.2214C>T
(ENOSF1)
|
|
|
NR_148711.1:n.2065C>T
(ENOSF1)
|
|
|
NR_148712.1:n.2398C>T
(ENOSF1)
|
|
|
XM_024451242.1:c.424-484G>A
(TYMS)
|
XP_024307010.1:n.424-484G>A
|
|
XR_002958180.1:n.1966C>T
(ENOSF1)
|
|
|
XR_430041.4:n.2352C>T
(ENOSF1)
|
|
|
NM_001071.4:c.805-484G>A
(TYMS)
MANE Select
|
NP_001062.1:n.805-484G>A
|
|
NM_017512.7:c.*1929C>T
(ENOSF1)
MANE Select
|
NP_059982.2:n.*1929C>T
|
|
NM_001318760.2:c.*1929C>T
(ENOSF1)
|
NP_001305689.1:n.*1929C>T
|
|
NM_001354065.2:c.*1929C>T
(ENOSF1)
|
NP_001340994.1:n.*1929C>T
|
|
NM_001354066.2:c.*1929C>T
(ENOSF1)
|
NP_001340995.1:n.*1929C>T
|
|
NM_001354067.2:c.*1929C>T
(ENOSF1)
|
NP_001340996.1:n.*1929C>T
|
|
NM_001354068.2:c.*1929C>T
(ENOSF1)
|
NP_001340997.1:n.*1929C>T
|
|
NM_001354867.2:c.703-484G>A
(TYMS)
|
NP_001341796.1:n.703-484G>A
|
|
NM_001354868.2:c.556-484G>A
(TYMS)
|
NP_001341797.1:n.556-484G>A
|
|
NM_202758.5:c.*1929C>T
(ENOSF1)
|
NP_974487.2:n.*1929C>T
|
|
NR_148706.2:n.2104C>T
(ENOSF1)
|
|
|
NR_148707.2:n.2220C>T
(ENOSF1)
|
|
|
NR_148708.2:n.2468C>T
(ENOSF1)
|
|
|
NR_148709.2:n.2154C>T
(ENOSF1)
|
|
|
NR_148710.2:n.2180C>T
(ENOSF1)
|
|
|
NR_148711.2:n.2031C>T
(ENOSF1)
|
|
|
NR_148712.2:n.2364C>T
(ENOSF1)
|
|
|