ENST00000323274.15:c.805-487A>C
(TYMS)
MANE Select
|
ENSP00000315644.10:n.805-487A>C
|
|
ENST00000647584.2:c.*1932T>G
(ENOSF1)
MANE Select
|
ENSP00000497230.2:n.*1932T>G
|
|
ENST00000323224.7:c.703-487A>C
(TYMS)
|
ENSP00000314727.7:n.703-487A>C
|
|
ENST00000323250.9:c.556-487A>C
(TYMS)
|
ENSP00000314902.5:n.556-487A>C
|
|
ENST00000323274.14:c.805-487A>C
(TYMS)
|
ENSP00000315644.10:n.805-487A>C
|
|
ENST00000383578.7:c.*848T>G
(ENOSF1)
|
ENSP00000373072.3:n.*848T>G
|
|
ENST00000581920.1:n.383-487A>C
(TYMS)
|
|
|
ENST00000584259.6:n.4291T>G
(ENOSF1)
|
|
|
NM_001071.2:c.805-487A>C , LRG_783t1:c.805-487A>C
(TYMS)
|
NP_001062.1:n.805-487A>C
|
|
NM_001126123.3:c.*848T>G
(ENOSF1)
|
NP_001119595.1:n.*848T>G
|
|
NM_017512.5:c.*1932T>G
(ENOSF1)
|
NP_059982.2:n.*1932T>G
|
|
NM_202758.3:c.*1932T>G
(ENOSF1)
|
NP_974487.1:n.*1932T>G
|
|
NM_001071.3:c.805-487A>C
(TYMS)
|
NP_001062.1:n.805-487A>C
|
|
NM_001354867.1:c.703-487A>C
(TYMS)
|
NP_001341796.1:n.703-487A>C
|
|
NM_001354868.1:c.556-487A>C
(TYMS)
|
NP_001341797.1:n.556-487A>C
|
|
NR_148706.1:n.2141T>G
(ENOSF1)
|
|
|
NR_148707.1:n.2257T>G
(ENOSF1)
|
|
|
NR_148708.1:n.2505T>G
(ENOSF1)
|
|
|
NR_148709.1:n.2191T>G
(ENOSF1)
|
|
|
NR_148710.1:n.2217T>G
(ENOSF1)
|
|
|
NR_148711.1:n.2068T>G
(ENOSF1)
|
|
|
NR_148712.1:n.2401T>G
(ENOSF1)
|
|
|
XM_024451242.1:c.424-487A>C
(TYMS)
|
XP_024307010.1:n.424-487A>C
|
|
XR_002958180.1:n.1969T>G
(ENOSF1)
|
|
|
XR_430041.4:n.2355T>G
(ENOSF1)
|
|
|
NM_001071.4:c.805-487A>C
(TYMS)
MANE Select
|
NP_001062.1:n.805-487A>C
|
|
NM_017512.7:c.*1932T>G
(ENOSF1)
MANE Select
|
NP_059982.2:n.*1932T>G
|
|
NM_001318760.2:c.*1932T>G
(ENOSF1)
|
NP_001305689.1:n.*1932T>G
|
|
NM_001354065.2:c.*1932T>G
(ENOSF1)
|
NP_001340994.1:n.*1932T>G
|
|
NM_001354066.2:c.*1932T>G
(ENOSF1)
|
NP_001340995.1:n.*1932T>G
|
|
NM_001354067.2:c.*1932T>G
(ENOSF1)
|
NP_001340996.1:n.*1932T>G
|
|
NM_001354068.2:c.*1932T>G
(ENOSF1)
|
NP_001340997.1:n.*1932T>G
|
|
NM_001354867.2:c.703-487A>C
(TYMS)
|
NP_001341796.1:n.703-487A>C
|
|
NM_001354868.2:c.556-487A>C
(TYMS)
|
NP_001341797.1:n.556-487A>C
|
|
NM_202758.5:c.*1932T>G
(ENOSF1)
|
NP_974487.2:n.*1932T>G
|
|
NR_148706.2:n.2107T>G
(ENOSF1)
|
|
|
NR_148707.2:n.2223T>G
(ENOSF1)
|
|
|
NR_148708.2:n.2471T>G
(ENOSF1)
|
|
|
NR_148709.2:n.2157T>G
(ENOSF1)
|
|
|
NR_148710.2:n.2183T>G
(ENOSF1)
|
|
|
NR_148711.2:n.2034T>G
(ENOSF1)
|
|
|
NR_148712.2:n.2367T>G
(ENOSF1)
|
|
|