ENST00000376585.6:c.*836T>C
(MTHFR)
|
ENSP00000365770.1:n.*836T>C
|
|
ENST00000376590.9:c.*836T>C
(MTHFR)
MANE Select
|
ENSP00000365775.3:n.*836T>C
|
|
ENST00000376592.6:c.*836T>C
(MTHFR)
|
ENSP00000365777.1:n.*836T>C
|
|
ENST00000641747.1:c.*2319T>C
(MTHFR)
|
ENSP00000493116.1:n.*2319T>C
|
|
ENST00000376583.7:c.2930T>C
(MTHFR)
|
ENSP00000365767.3:n.2930T>C
|
|
ENST00000376585.5:c.*836T>C
(MTHFR)
|
ENSP00000365770.1:n.*836T>C
|
|
ENST00000376590.7:c.*836T>C
(MTHFR)
|
ENSP00000365775.3:n.*836T>C
|
|
ENST00000376592.5:c.*836T>C
(MTHFR)
|
ENSP00000365777.1:n.*836T>C
|
|
NM_005957.4:c.*836T>C , LRG_726t1:c.*836T>C
(MTHFR)
|
NP_005948.3:n.*836T>C
|
|
NM_001330358.1:c.*836T>C
(MTHFR)
|
NP_001317287.1:n.*836T>C
|
|
XM_011541272.3:c.*398A>G
(C1orf167)
|
XP_011539574.1:n.*398A>G
|
|
XM_011541276.3:c.*385A>G
(C1orf167)
|
XP_011539578.1:n.*385A>G
|
|
XM_011541277.3:c.*398A>G
(C1orf167)
|
XP_011539579.1:n.*398A>G
|
|
XM_024446506.1:c.*801A>G
(C1orf167)
|
XP_024302274.1:n.*801A>G
|
|
XM_024446507.1:c.*801A>G
(C1orf167)
|
XP_024302275.1:n.*801A>G
|
|
XM_024446508.1:c.*801A>G
(C1orf167)
|
XP_024302276.1:n.*801A>G
|
|
XM_024446509.1:c.*801A>G
(C1orf167)
|
XP_024302277.1:n.*801A>G
|
|
XM_024446512.1:c.*801A>G
(C1orf167)
|
XP_024302280.1:n.*801A>G
|
|
XM_024446514.1:c.*801A>G
(C1orf167)
|
XP_024302282.1:n.*801A>G
|
|
XM_024446515.1:c.*801A>G
(C1orf167)
|
XP_024302283.1:n.*801A>G
|
|
XM_024446517.1:c.*801A>G
(C1orf167)
|
XP_024302285.1:n.*801A>G
|
|
XM_024446518.1:c.*801A>G
(C1orf167)
|
XP_024302286.1:n.*801A>G
|
|
NM_005957.5:c.*836T>C
(MTHFR)
MANE Select
|
NP_005948.3:n.*836T>C
|
|
NM_001330358.2:c.*836T>C
(MTHFR)
|
NP_001317287.1:n.*836T>C
|
|