ENST00000323274.15:c.841A>C
(TYMS)
MANE Select
|
ENSP00000315644.10:p.Ile281Leu
|
|
ENST00000647584.2:c.*1409T>G
(ENOSF1)
MANE Select
|
ENSP00000497230.2:n.*1409T>G
|
|
ENST00000323224.7:c.739A>C
(TYMS)
|
ENSP00000314727.7:p.Ile247Leu
|
|
ENST00000323250.9:c.592A>C
(TYMS)
|
ENSP00000314902.5:p.Ile198Leu
|
|
ENST00000323274.14:c.841A>C
(TYMS)
|
ENSP00000315644.10:p.Ile281Leu
|
|
ENST00000383578.7:c.*325T>G
(ENOSF1)
|
ENSP00000373072.3:n.*325T>G
|
|
ENST00000581920.1:n.419A>C
(TYMS)
|
|
|
ENST00000584259.6:n.3768T>G
(ENOSF1)
|
|
|
NM_001071.2:c.841A>C , LRG_783t1:c.841A>C
(TYMS)
|
NP_001062.1:p.Ile281Leu
|
|
NM_001126123.3:c.*325T>G
(ENOSF1)
|
NP_001119595.1:n.*325T>G
|
|
NM_017512.5:c.*1409T>G
(ENOSF1)
|
NP_059982.2:n.*1409T>G
|
|
NM_202758.3:c.*1409T>G
(ENOSF1)
|
NP_974487.1:n.*1409T>G
|
|
XR_243810.3:n.1693T>G
(ENOSF1)
|
|
|
XR_243811.2:n.1718T>G
(ENOSF1)
|
|
|
XR_430041.2:n.1813T>G
(ENOSF1)
|
|
|
NM_001071.3:c.841A>C
(TYMS)
|
NP_001062.1:p.Ile281Leu
|
|
NM_001354867.1:c.739A>C
(TYMS)
|
NP_001341796.1:p.Ile247Leu
|
|
NM_001354868.1:c.592A>C
(TYMS)
|
NP_001341797.1:p.Ile198Leu
|
|
NR_148706.1:n.1618T>G
(ENOSF1)
|
|
|
NR_148707.1:n.1734T>G
(ENOSF1)
|
|
|
NR_148708.1:n.1982T>G
(ENOSF1)
|
|
|
NR_148709.1:n.1668T>G
(ENOSF1)
|
|
|
NR_148710.1:n.1694T>G
(ENOSF1)
|
|
|
NR_148711.1:n.1545T>G
(ENOSF1)
|
|
|
NR_148712.1:n.1878T>G
(ENOSF1)
|
|
|
XM_024451242.1:c.460A>C
(TYMS)
|
XP_024307010.1:p.Ile154Leu
|
|
XR_002958180.1:n.1446T>G
(ENOSF1)
|
|
|
XR_430041.4:n.1832T>G
(ENOSF1)
|
|
|
NM_001071.4:c.841A>C
(TYMS)
MANE Select
|
NP_001062.1:p.Ile281Leu
|
|
NM_017512.7:c.*1409T>G
(ENOSF1)
MANE Select
|
NP_059982.2:n.*1409T>G
|
|
NM_001318760.2:c.*1409T>G
(ENOSF1)
|
NP_001305689.1:n.*1409T>G
|
|
NM_001354065.2:c.*1409T>G
(ENOSF1)
|
NP_001340994.1:n.*1409T>G
|
|
NM_001354066.2:c.*1409T>G
(ENOSF1)
|
NP_001340995.1:n.*1409T>G
|
|
NM_001354067.2:c.*1409T>G
(ENOSF1)
|
NP_001340996.1:n.*1409T>G
|
|
NM_001354068.2:c.*1409T>G
(ENOSF1)
|
NP_001340997.1:n.*1409T>G
|
|
NM_001354867.2:c.739A>C
(TYMS)
|
NP_001341796.1:p.Ile247Leu
|
|
NM_001354868.2:c.592A>C
(TYMS)
|
NP_001341797.1:p.Ile198Leu
|
|
NM_202758.5:c.*1409T>G
(ENOSF1)
|
NP_974487.2:n.*1409T>G
|
|
NR_148706.2:n.1584T>G
(ENOSF1)
|
|
|
NR_148707.2:n.1700T>G
(ENOSF1)
|
|
|
NR_148708.2:n.1948T>G
(ENOSF1)
|
|
|
NR_148709.2:n.1634T>G
(ENOSF1)
|
|
|
NR_148710.2:n.1660T>G
(ENOSF1)
|
|
|
NR_148711.2:n.1511T>G
(ENOSF1)
|
|
|
NR_148712.2:n.1844T>G
(ENOSF1)
|
|
|