ENST00000323274.15:c.805-567T>G
(TYMS)
MANE Select
|
ENSP00000315644.10:n.805-567T>G
|
|
ENST00000647584.2:c.*2012A>C
(ENOSF1)
MANE Select
|
ENSP00000497230.2:n.*2012A>C
|
|
ENST00000323224.7:c.703-567T>G
(TYMS)
|
ENSP00000314727.7:n.703-567T>G
|
|
ENST00000323250.9:c.556-567T>G
(TYMS)
|
ENSP00000314902.5:n.556-567T>G
|
|
ENST00000323274.14:c.805-567T>G
(TYMS)
|
ENSP00000315644.10:n.805-567T>G
|
|
ENST00000383578.7:c.*928A>C
(ENOSF1)
|
ENSP00000373072.3:n.*928A>C
|
|
ENST00000581920.1:n.383-567T>G
(TYMS)
|
|
|
ENST00000584259.6:n.4371A>C
(ENOSF1)
|
|
|
NM_001071.2:c.805-567T>G , LRG_783t1:c.805-567T>G
(TYMS)
|
NP_001062.1:n.805-567T>G
|
|
NM_001126123.3:c.*928A>C
(ENOSF1)
|
NP_001119595.1:n.*928A>C
|
|
NM_017512.5:c.*2012A>C
(ENOSF1)
|
NP_059982.2:n.*2012A>C
|
|
NM_202758.3:c.*2012A>C
(ENOSF1)
|
NP_974487.1:n.*2012A>C
|
|
NM_001071.3:c.805-567T>G
(TYMS)
|
NP_001062.1:n.805-567T>G
|
|
NM_001354867.1:c.703-567T>G
(TYMS)
|
NP_001341796.1:n.703-567T>G
|
|
NM_001354868.1:c.556-567T>G
(TYMS)
|
NP_001341797.1:n.556-567T>G
|
|
NR_148706.1:n.2221A>C
(ENOSF1)
|
|
|
NR_148707.1:n.2337A>C
(ENOSF1)
|
|
|
NR_148708.1:n.2585A>C
(ENOSF1)
|
|
|
NR_148709.1:n.2271A>C
(ENOSF1)
|
|
|
NR_148710.1:n.2297A>C
(ENOSF1)
|
|
|
NR_148711.1:n.2148A>C
(ENOSF1)
|
|
|
NR_148712.1:n.2481A>C
(ENOSF1)
|
|
|
XM_024451242.1:c.424-567T>G
(TYMS)
|
XP_024307010.1:n.424-567T>G
|
|
XR_002958180.1:n.2049A>C
(ENOSF1)
|
|
|
XR_430041.4:n.2435A>C
(ENOSF1)
|
|
|
NM_001071.4:c.805-567T>G
(TYMS)
MANE Select
|
NP_001062.1:n.805-567T>G
|
|
NM_017512.7:c.*2012A>C
(ENOSF1)
MANE Select
|
NP_059982.2:n.*2012A>C
|
|
NM_001318760.2:c.*2012A>C
(ENOSF1)
|
NP_001305689.1:n.*2012A>C
|
|
NM_001354065.2:c.*2012A>C
(ENOSF1)
|
NP_001340994.1:n.*2012A>C
|
|
NM_001354066.2:c.*2012A>C
(ENOSF1)
|
NP_001340995.1:n.*2012A>C
|
|
NM_001354067.2:c.*2012A>C
(ENOSF1)
|
NP_001340996.1:n.*2012A>C
|
|
NM_001354068.2:c.*2012A>C
(ENOSF1)
|
NP_001340997.1:n.*2012A>C
|
|
NM_001354867.2:c.703-567T>G
(TYMS)
|
NP_001341796.1:n.703-567T>G
|
|
NM_001354868.2:c.556-567T>G
(TYMS)
|
NP_001341797.1:n.556-567T>G
|
|
NM_202758.5:c.*2012A>C
(ENOSF1)
|
NP_974487.2:n.*2012A>C
|
|
NR_148706.2:n.2187A>C
(ENOSF1)
|
|
|
NR_148707.2:n.2303A>C
(ENOSF1)
|
|
|
NR_148708.2:n.2551A>C
(ENOSF1)
|
|
|
NR_148709.2:n.2237A>C
(ENOSF1)
|
|
|
NR_148710.2:n.2263A>C
(ENOSF1)
|
|
|
NR_148711.2:n.2114A>C
(ENOSF1)
|
|
|
NR_148712.2:n.2447A>C
(ENOSF1)
|
|
|