ENST00000323274.15:c.827T>C
(TYMS)
MANE Select
|
ENSP00000315644.10:p.Phe276Ser
|
|
ENST00000647584.2:c.*1423A>G
(ENOSF1)
MANE Select
|
ENSP00000497230.2:n.*1423A>G
|
|
ENST00000323224.7:c.725T>C
(TYMS)
|
ENSP00000314727.7:p.Phe242Ser
|
|
ENST00000323250.9:c.578T>C
(TYMS)
|
ENSP00000314902.5:p.Phe193Ser
|
|
ENST00000323274.14:c.827T>C
(TYMS)
|
ENSP00000315644.10:p.Phe276Ser
|
|
ENST00000383578.7:c.*339A>G
(ENOSF1)
|
ENSP00000373072.3:n.*339A>G
|
|
ENST00000581920.1:n.405T>C
(TYMS)
|
|
|
ENST00000584259.6:n.3782A>G
(ENOSF1)
|
|
|
NM_001071.2:c.827T>C , LRG_783t1:c.827T>C
(TYMS)
|
NP_001062.1:p.Phe276Ser
|
|
NM_001126123.3:c.*339A>G
(ENOSF1)
|
NP_001119595.1:n.*339A>G
|
|
NM_017512.5:c.*1423A>G
(ENOSF1)
|
NP_059982.2:n.*1423A>G
|
|
NM_202758.3:c.*1423A>G
(ENOSF1)
|
NP_974487.1:n.*1423A>G
|
|
XR_243810.3:n.1707A>G
(ENOSF1)
|
|
|
XR_243811.2:n.1732A>G
(ENOSF1)
|
|
|
XR_430041.2:n.1827A>G
(ENOSF1)
|
|
|
NM_001071.3:c.827T>C
(TYMS)
|
NP_001062.1:p.Phe276Ser
|
|
NM_001354867.1:c.725T>C
(TYMS)
|
NP_001341796.1:p.Phe242Ser
|
|
NM_001354868.1:c.578T>C
(TYMS)
|
NP_001341797.1:p.Phe193Ser
|
|
NR_148706.1:n.1632A>G
(ENOSF1)
|
|
|
NR_148707.1:n.1748A>G
(ENOSF1)
|
|
|
NR_148708.1:n.1996A>G
(ENOSF1)
|
|
|
NR_148709.1:n.1682A>G
(ENOSF1)
|
|
|
NR_148710.1:n.1708A>G
(ENOSF1)
|
|
|
NR_148711.1:n.1559A>G
(ENOSF1)
|
|
|
NR_148712.1:n.1892A>G
(ENOSF1)
|
|
|
XM_024451242.1:c.446T>C
(TYMS)
|
XP_024307010.1:p.Phe149Ser
|
|
XR_002958180.1:n.1460A>G
(ENOSF1)
|
|
|
XR_430041.4:n.1846A>G
(ENOSF1)
|
|
|
NM_001071.4:c.827T>C
(TYMS)
MANE Select
|
NP_001062.1:p.Phe276Ser
|
|
NM_017512.7:c.*1423A>G
(ENOSF1)
MANE Select
|
NP_059982.2:n.*1423A>G
|
|
NM_001318760.2:c.*1423A>G
(ENOSF1)
|
NP_001305689.1:n.*1423A>G
|
|
NM_001354065.2:c.*1423A>G
(ENOSF1)
|
NP_001340994.1:n.*1423A>G
|
|
NM_001354066.2:c.*1423A>G
(ENOSF1)
|
NP_001340995.1:n.*1423A>G
|
|
NM_001354067.2:c.*1423A>G
(ENOSF1)
|
NP_001340996.1:n.*1423A>G
|
|
NM_001354068.2:c.*1423A>G
(ENOSF1)
|
NP_001340997.1:n.*1423A>G
|
|
NM_001354867.2:c.725T>C
(TYMS)
|
NP_001341796.1:p.Phe242Ser
|
|
NM_001354868.2:c.578T>C
(TYMS)
|
NP_001341797.1:p.Phe193Ser
|
|
NM_202758.5:c.*1423A>G
(ENOSF1)
|
NP_974487.2:n.*1423A>G
|
|
NR_148706.2:n.1598A>G
(ENOSF1)
|
|
|
NR_148707.2:n.1714A>G
(ENOSF1)
|
|
|
NR_148708.2:n.1962A>G
(ENOSF1)
|
|
|
NR_148709.2:n.1648A>G
(ENOSF1)
|
|
|
NR_148710.2:n.1674A>G
(ENOSF1)
|
|
|
NR_148711.2:n.1525A>G
(ENOSF1)
|
|
|
NR_148712.2:n.1858A>G
(ENOSF1)
|
|
|