ENST00000323274.15:c.809A>C
(TYMS)
MANE Select
|
ENSP00000315644.10:p.Gln270Pro
|
|
ENST00000647584.2:c.*1441T>G
(ENOSF1)
MANE Select
|
ENSP00000497230.2:n.*1441T>G
|
|
ENST00000323224.7:c.707A>C
(TYMS)
|
ENSP00000314727.7:p.Gln236Pro
|
|
ENST00000323250.9:c.560A>C
(TYMS)
|
ENSP00000314902.5:p.Gln187Pro
|
|
ENST00000323274.14:c.809A>C
(TYMS)
|
ENSP00000315644.10:p.Gln270Pro
|
|
ENST00000383578.7:c.*357T>G
(ENOSF1)
|
ENSP00000373072.3:n.*357T>G
|
|
ENST00000581920.1:n.387A>C
(TYMS)
|
|
|
ENST00000584259.6:n.3800T>G
(ENOSF1)
|
|
|
NM_001071.2:c.809A>C , LRG_783t1:c.809A>C
(TYMS)
|
NP_001062.1:p.Gln270Pro
|
|
NM_001126123.3:c.*357T>G
(ENOSF1)
|
NP_001119595.1:n.*357T>G
|
|
NM_017512.5:c.*1441T>G
(ENOSF1)
|
NP_059982.2:n.*1441T>G
|
|
NM_202758.3:c.*1441T>G
(ENOSF1)
|
NP_974487.1:n.*1441T>G
|
|
XR_243810.3:n.1725T>G
(ENOSF1)
|
|
|
XR_243811.2:n.1750T>G
(ENOSF1)
|
|
|
XR_430041.2:n.1845T>G
(ENOSF1)
|
|
|
NM_001071.3:c.809A>C
(TYMS)
|
NP_001062.1:p.Gln270Pro
|
|
NM_001354867.1:c.707A>C
(TYMS)
|
NP_001341796.1:p.Gln236Pro
|
|
NM_001354868.1:c.560A>C
(TYMS)
|
NP_001341797.1:p.Gln187Pro
|
|
NR_148706.1:n.1650T>G
(ENOSF1)
|
|
|
NR_148707.1:n.1766T>G
(ENOSF1)
|
|
|
NR_148708.1:n.2014T>G
(ENOSF1)
|
|
|
NR_148709.1:n.1700T>G
(ENOSF1)
|
|
|
NR_148710.1:n.1726T>G
(ENOSF1)
|
|
|
NR_148711.1:n.1577T>G
(ENOSF1)
|
|
|
NR_148712.1:n.1910T>G
(ENOSF1)
|
|
|
XM_024451242.1:c.428A>C
(TYMS)
|
XP_024307010.1:p.Gln143Pro
|
|
XR_002958180.1:n.1478T>G
(ENOSF1)
|
|
|
XR_430041.4:n.1864T>G
(ENOSF1)
|
|
|
NM_001071.4:c.809A>C
(TYMS)
MANE Select
|
NP_001062.1:p.Gln270Pro
|
|
NM_017512.7:c.*1441T>G
(ENOSF1)
MANE Select
|
NP_059982.2:n.*1441T>G
|
|
NM_001318760.2:c.*1441T>G
(ENOSF1)
|
NP_001305689.1:n.*1441T>G
|
|
NM_001354065.2:c.*1441T>G
(ENOSF1)
|
NP_001340994.1:n.*1441T>G
|
|
NM_001354066.2:c.*1441T>G
(ENOSF1)
|
NP_001340995.1:n.*1441T>G
|
|
NM_001354067.2:c.*1441T>G
(ENOSF1)
|
NP_001340996.1:n.*1441T>G
|
|
NM_001354068.2:c.*1441T>G
(ENOSF1)
|
NP_001340997.1:n.*1441T>G
|
|
NM_001354867.2:c.707A>C
(TYMS)
|
NP_001341796.1:p.Gln236Pro
|
|
NM_001354868.2:c.560A>C
(TYMS)
|
NP_001341797.1:p.Gln187Pro
|
|
NM_202758.5:c.*1441T>G
(ENOSF1)
|
NP_974487.2:n.*1441T>G
|
|
NR_148706.2:n.1616T>G
(ENOSF1)
|
|
|
NR_148707.2:n.1732T>G
(ENOSF1)
|
|
|
NR_148708.2:n.1980T>G
(ENOSF1)
|
|
|
NR_148709.2:n.1666T>G
(ENOSF1)
|
|
|
NR_148710.2:n.1692T>G
(ENOSF1)
|
|
|
NR_148711.2:n.1543T>G
(ENOSF1)
|
|
|
NR_148712.2:n.1876T>G
(ENOSF1)
|
|
|