ENST00000395925.8:c.3309G>C
MANE Select
|
ENSP00000379258.3:p.Gln1103His
|
|
ENST00000677288.1:c.3135G>C
|
ENSP00000503986.1:p.Gln1045His
|
|
ENST00000677605.1:c.3309G>C
|
ENSP00000503743.1:p.Gln1103His
|
|
ENST00000678429.1:c.3309G>C
|
ENSP00000502957.1:p.Gln1103His
|
|
ENST00000395925.7:c.3309G>C
|
ENSP00000379258.3:p.Gln1103His
|
|
ENST00000479210.1:n.3286G>C
|
|
|
NM_000168.5:c.3309G>C
|
NP_000159.3:p.Gln1103His
|
|
XM_005249703.1:c.3309G>C
|
XP_005249760.1:p.Gln1103His
|
|
XM_005249704.2:c.3309G>C
|
XP_005249761.1:p.Gln1103His
|
|
XM_011515272.1:c.3309G>C
|
XP_011513574.1:p.Gln1103His
|
|
XM_011515273.1:c.3309G>C
|
XP_011513575.1:p.Gln1103His
|
|
XM_011515274.1:c.3132G>C
|
XP_011513576.1:p.Gln1044His
|
|
XM_011515274.2:c.3132G>C
|
XP_011513576.1:p.Gln1044His
|
|
XM_017011997.1:c.3306G>C
|
XP_016867486.1:p.Gln1102His
|
|
NM_000168.6:c.3309G>C
MANE Select
|
NP_000159.3:p.Gln1103His
|
|