|
NM_001953.5:c.1402G>T
(TYMP)
MANE Select
|
NP_001944.1:p.Ala468Ser
|
|
ENST00000252029.8:c.1402G>T
(TYMP)
MANE Select
|
ENSP00000252029.3:p.Ala468Ser
|
|
NM_001113755.2:c.1402G>T
(TYMP)
|
NP_001107227.1:p.Ala468Ser
|
|
NM_001113755.3:c.1402G>T
(TYMP)
|
NP_001107227.1:p.Ala468Ser
|
|
NM_001113756.2:c.1402G>T
(TYMP)
|
NP_001107228.1:p.Ala468Ser
|
|
NM_001113756.3:c.1402G>T
(TYMP)
|
NP_001107228.1:p.Ala468Ser
|
|
NM_001169109.1:c.-14+429G>T
(SCO2)
|
NP_001162580.1:n.-14+429G>T
|
|
NM_001169109.2:c.-14+429G>T
(SCO2)
|
NP_001162580.1:n.-14+429G>T
|
|
NM_001169110.1:c.-14+184G>T
(SCO2)
|
NP_001162581.1:n.-14+184G>T
|
|
NM_001257988.1:c.1402G>T , LRG_727t1:c.1402G>T
(TYMP)
|
NP_001244917.1:p.Ala468Ser
|
|
NM_001257989.1:c.1417G>T , LRG_727t2:c.1417G>T
(TYMP)
|
NP_001244918.1:p.Ala473Ser
|
|
NM_001953.4:c.1402G>T
(TYMP)
|
NP_001944.1:p.Ala468Ser
|
|
ENST00000252029.7:c.1402G>T
(TYMP)
|
ENSP00000252029.3:p.Ala468Ser
|
|
ENST00000395678.7:c.1402G>T
(TYMP)
|
ENSP00000379036.3:p.Ala468Ser
|
|
ENST00000395680.5:c.1402G>T
(TYMP)
|
ENSP00000379037.1:p.Ala468Ser
|
|
ENST00000395680.6:c.1402G>T
(TYMP)
|
ENSP00000379037.1:p.Ala468Ser
|
|
ENST00000395681.5:c.1417G>T
(TYMP)
|
ENSP00000379038.1:p.Ala473Ser
|
|
ENST00000395681.6:c.1417G>T
(TYMP)
|
ENSP00000379038.1:p.Ala473Ser
|
|
ENST00000423348.1:c.-14+429G>T
|
ENSP00000403570.1:n.-14+429G>T
|
|
ENST00000425169.1:c.1303G>T
(TYMP)
|
ENSP00000395875.1:p.Ala435Ser
|
|
ENST00000439934.5:c.-14+184G>T
|
ENSP00000415642.1:n.-14+184G>T
|
|
ENST00000476284.1:n.1512G>T
(TYMP)
|
|
|
ENST00000487577.5:n.1689G>T
(TYMP)
|
|
|
ENST00000535425.5:c.-14+184G>T
|
ENSP00000444242.1:n.-14+184G>T
|
|
ENST00000543927.5:c.-14+429G>T
|
ENSP00000444433.1:n.-14+429G>T
|
|
ENST00000543927.6:c.-14+429G>T
(SCO2)
|
ENSP00000444433.1:n.-14+429G>T
|
|
ENST00000638598.2:c.-14+184G>T
(SCO2)
|
ENSP00000491753.2:n.-14+184G>T
|
|
ENST00000651490.1:c.194G>T
(TYMP)
|
|
