|
ENST00000504073.2:c.611T>G
|
ENSP00000422030.2:p.Val204Gly
|
|
|
ENST00000511303.6:n.310-484T>G
|
|
|
|
ENST00000512526.2:c.576-484T>G
|
ENSP00000426606.2:n.576-484T>G
|
|
|
ENST00000682109.1:c.641T>G
|
ENSP00000508041.1:p.Val214Gly
|
|
|
ENST00000683226.1:n.1359T>G
|
|
|
|
ENST00000683294.1:c.*27T>G
|
ENSP00000508134.1:n.*27T>G
|
|
|
ENST00000683544.1:n.127T>G
|
|
|
|
ENST00000262018.8:c.761T>G
MANE Select
|
ENSP00000262018.3:p.Val254Gly
|
|
|
ENST00000262018.7:c.761T>G
|
ENSP00000262018.3:p.Val254Gly
|
|
|
ENST00000344627.10:c.585-484T>G
|
ENSP00000345522.6:n.585-484T>G
|
|
|
ENST00000504073.1:c.78T>G
|
|
|
|
ENST00000511303.5:c.306-484T>G
|
ENSP00000426104.1:n.306-484T>G
|
|
|
ENST00000512526.1:c.420-484T>G
|
|
|
|
ENST00000513821.5:c.748-484T>G
|
ENSP00000426571.1:n.748-484T>G
|
|
|
ENST00000513942.5:n.376-484T>G
|
|
|
|
NM_000023.2:c.761T>G , LRG_203t1:c.761T>G
|
NP_000014.1:p.Val254Gly
|
|
|
NM_001135697.1:c.585-484T>G
|
NP_001129169.1:n.585-484T>G
|
|
|
XM_011525120.1:c.761T>G
|
XP_011523422.1:p.Val254Gly
|
|
|
XM_011525121.1:c.611T>G
|
XP_011523423.1:p.Val204Gly
|
|
|
XM_011525122.1:c.748-484T>G
|
XP_011523424.1:n.748-484T>G
|
|
|
XM_011525123.1:c.585-484T>G
|
XP_011523425.1:n.585-484T>G
|
|
|
XM_011525124.1:c.455T>G
|
XP_011523426.1:p.Val152Gly
|
|
|
XR_934517.1:n.814-484T>G
|
|
|
|
NM_000023.3:c.761T>G
|
NP_000014.1:p.Val254Gly
|
|
|
NM_001135697.2:c.585-484T>G
|
NP_001129169.1:n.585-484T>G
|
|
|
NR_135553.1:n.804-484T>G
|
|
|
|
XM_011525120.2:c.923T>G
|
XP_011523422.2:p.Val308Gly
|
|
|
XM_011525121.2:c.773T>G
|
XP_011523423.2:p.Val258Gly
|
|
|
XM_011525122.2:c.910-484T>G
|
XP_011523424.2:n.910-484T>G
|
|
|
XM_011525123.2:c.747-484T>G
|
XP_011523425.2:n.747-484T>G
|
|
|
XM_011525124.2:c.455T>G
|
XP_011523426.1:p.Val152Gly
|
|
|
XM_024450873.1:c.455T>G
|
XP_024306641.1:p.Val152Gly
|
|
|
XR_002958056.1:n.1358T>G
|
|
|
|
NM_000023.4:c.761T>G
MANE Select
|
NP_000014.1:p.Val254Gly
|
|
|
NM_001135697.3:c.585-484T>G
|
NP_001129169.1:n.585-484T>G
|
|
|
NR_135553.2:n.784-484T>G
|
|
|
