ENST00000323274.15:c.817C>T
(TYMS)
MANE Select
|
ENSP00000315644.10:p.Pro273Ser
|
|
ENST00000647584.2:c.*1433G>A
(ENOSF1)
MANE Select
|
ENSP00000497230.2:n.*1433G>A
|
|
ENST00000323224.7:c.715C>T
(TYMS)
|
ENSP00000314727.7:p.Pro239Ser
|
|
ENST00000323250.9:c.568C>T
(TYMS)
|
ENSP00000314902.5:p.Pro190Ser
|
|
ENST00000323274.14:c.817C>T
(TYMS)
|
ENSP00000315644.10:p.Pro273Ser
|
|
ENST00000383578.7:c.*349G>A
(ENOSF1)
|
ENSP00000373072.3:n.*349G>A
|
|
ENST00000581920.1:n.395C>T
(TYMS)
|
|
|
ENST00000584259.6:n.3792G>A
(ENOSF1)
|
|
|
NM_001071.2:c.817C>T , LRG_783t1:c.817C>T
(TYMS)
|
NP_001062.1:p.Pro273Ser
|
|
NM_001126123.3:c.*349G>A
(ENOSF1)
|
NP_001119595.1:n.*349G>A
|
|
NM_017512.5:c.*1433G>A
(ENOSF1)
|
NP_059982.2:n.*1433G>A
|
|
NM_202758.3:c.*1433G>A
(ENOSF1)
|
NP_974487.1:n.*1433G>A
|
|
XR_243810.3:n.1717G>A
(ENOSF1)
|
|
|
XR_243811.2:n.1742G>A
(ENOSF1)
|
|
|
XR_430041.2:n.1837G>A
(ENOSF1)
|
|
|
NM_001071.3:c.817C>T
(TYMS)
|
NP_001062.1:p.Pro273Ser
|
|
NM_001354867.1:c.715C>T
(TYMS)
|
NP_001341796.1:p.Pro239Ser
|
|
NM_001354868.1:c.568C>T
(TYMS)
|
NP_001341797.1:p.Pro190Ser
|
|
NR_148706.1:n.1642G>A
(ENOSF1)
|
|
|
NR_148707.1:n.1758G>A
(ENOSF1)
|
|
|
NR_148708.1:n.2006G>A
(ENOSF1)
|
|
|
NR_148709.1:n.1692G>A
(ENOSF1)
|
|
|
NR_148710.1:n.1718G>A
(ENOSF1)
|
|
|
NR_148711.1:n.1569G>A
(ENOSF1)
|
|
|
NR_148712.1:n.1902G>A
(ENOSF1)
|
|
|
XM_024451242.1:c.436C>T
(TYMS)
|
XP_024307010.1:p.Pro146Ser
|
|
XR_002958180.1:n.1470G>A
(ENOSF1)
|
|
|
XR_430041.4:n.1856G>A
(ENOSF1)
|
|
|
NM_001071.4:c.817C>T
(TYMS)
MANE Select
|
NP_001062.1:p.Pro273Ser
|
|
NM_017512.7:c.*1433G>A
(ENOSF1)
MANE Select
|
NP_059982.2:n.*1433G>A
|
|
NM_001318760.2:c.*1433G>A
(ENOSF1)
|
NP_001305689.1:n.*1433G>A
|
|
NM_001354065.2:c.*1433G>A
(ENOSF1)
|
NP_001340994.1:n.*1433G>A
|
|
NM_001354066.2:c.*1433G>A
(ENOSF1)
|
NP_001340995.1:n.*1433G>A
|
|
NM_001354067.2:c.*1433G>A
(ENOSF1)
|
NP_001340996.1:n.*1433G>A
|
|
NM_001354068.2:c.*1433G>A
(ENOSF1)
|
NP_001340997.1:n.*1433G>A
|
|
NM_001354867.2:c.715C>T
(TYMS)
|
NP_001341796.1:p.Pro239Ser
|
|
NM_001354868.2:c.568C>T
(TYMS)
|
NP_001341797.1:p.Pro190Ser
|
|
NM_202758.5:c.*1433G>A
(ENOSF1)
|
NP_974487.2:n.*1433G>A
|
|
NR_148706.2:n.1608G>A
(ENOSF1)
|
|
|
NR_148707.2:n.1724G>A
(ENOSF1)
|
|
|
NR_148708.2:n.1972G>A
(ENOSF1)
|
|
|
NR_148709.2:n.1658G>A
(ENOSF1)
|
|
|
NR_148710.2:n.1684G>A
(ENOSF1)
|
|
|
NR_148711.2:n.1535G>A
(ENOSF1)
|
|
|
NR_148712.2:n.1868G>A
(ENOSF1)
|
|
|