ENST00000405460.9:c.9152C>T
MANE Select
|
ENSP00000384582.2:p.Ser3051Phe
|
|
ENST00000639431.1:c.265+36187C>T
|
ENSP00000491057.1:n.265+36187C>T
|
|
ENST00000639473.1:n.4611C>T
|
|
|
ENST00000640012.1:c.2959C>T
|
|
|
ENST00000640374.1:n.2296C>T
|
|
|
ENST00000640779.1:c.3881C>T
|
|
|
ENST00000405460.6:c.9152C>T
|
ENSP00000384582.2:p.Ser3051Phe
|
|
ENST00000509621.1:c.1849C>T
|
|
|
NM_032119.3:c.9152C>T
|
NP_115495.3:p.Ser3051Phe
|
|
NR_003149.1:n.9165C>T
|
|
|
XM_011543675.1:c.9149C>T
|
XP_011541977.1:p.Ser3050Phe
|
|
XM_011543676.1:c.9071C>T
|
XP_011541978.1:p.Ser3024Phe
|
|
XM_011543677.1:c.6455C>T
|
XP_011541979.1:p.Ser2152Phe
|
|
XM_011543678.1:c.9152C>T
|
XP_011541980.1:p.Ser3051Phe
|
|
XM_011543679.1:c.9152C>T
|
XP_011541981.1:p.Ser3051Phe
|
|
XR_948560.1:n.450G>A
|
|
|
NM_032119.4:c.9152C>T
MANE Select
|
NP_115495.3:p.Ser3051Phe
|
|
XM_017009963.2:c.9173C>T
|
XP_016865452.1:p.Ser3058Phe
|
|
XM_017009964.2:c.9170C>T
|
XP_016865453.1:p.Ser3057Phe
|
|
XM_017009965.1:c.9170C>T
|
XP_016865454.1:p.Ser3057Phe
|
|
XM_017009966.2:c.9092C>T
|
XP_016865455.1:p.Ser3031Phe
|
|
XM_017009967.1:c.9077C>T
|
XP_016865456.1:p.Ser3026Phe
|
|
XM_017009968.2:c.9173C>T
|
XP_016865457.1:p.Ser3058Phe
|
|
XM_017009969.2:c.9173C>T
|
XP_016865458.1:p.Ser3058Phe
|
|
XM_017009970.2:c.9173C>T
|
XP_016865459.1:p.Ser3058Phe
|
|
XM_017009971.2:c.9173C>T
|
XP_016865460.1:p.Ser3058Phe
|
|
XM_017009972.1:c.2291C>T
|
XP_016865461.1:p.Ser764Phe
|
|
XM_017009973.1:c.2270C>T
|
XP_016865462.1:p.Ser757Phe
|
|
XM_017009974.2:c.9173C>T
|
XP_016865463.1:p.Ser3058Phe
|
|
NR_003149.2:n.9168C>T
|
|
|