ENST00000338896.11:c.681-440G>T
MANE Select
|
ENSP00000344563.5:n.681-440G>T
|
|
ENST00000338896.10:c.681-440G>T
|
ENSP00000344563.5:n.681-440G>T
|
|
ENST00000338896.9:c.681-440G>T
|
ENSP00000344563.5:n.681-440G>T
|
|
ENST00000396502.5:c.*2145G>T
|
ENSP00000379759.1:n.*2145G>T
|
|
ENST00000539155.1:c.*2638G>T
|
ENSP00000444909.1:n.*2638G>T
|
|
ENST00000544853.5:c.*129-440G>T
|
ENSP00000439561.1:n.*129-440G>T
|
|
NM_001129998.1:c.681-440G>T
|
NP_001123470.1:n.681-440G>T
|
|
NM_205852.2:c.*2145G>T
|
NP_995324.2:n.*2145G>T
|
|
NR_120484.1:n.249-2118C>A
|
|
|
XM_006719070.2:c.681-527G>T
|
XP_006719133.1:n.681-527G>T
|
|
XM_006719071.2:c.*3-440G>T
|
XP_006719134.1:n.*3-440G>T
|
|
XM_006719072.1:c.*918G>T
|
XP_006719135.1:n.*918G>T
|
|
XM_011520658.1:c.654-440G>T
|
XP_011518960.1:n.654-440G>T
|
|
XM_011520659.1:c.*894G>T
|
XP_011518961.1:n.*894G>T
|
|
XM_011520660.1:c.*889G>T
|
XP_011518962.1:n.*889G>T
|
|
XM_011520661.1:c.*10-440G>T
|
XP_011518963.1:n.*10-440G>T
|
|
XM_011520662.1:c.*925G>T
|
XP_011518964.1:n.*925G>T
|
|
XM_011520663.1:c.526-440G>T
|
XP_011518965.1:n.526-440G>T
|
|
XM_011520664.1:c.526-527G>T
|
XP_011518966.1:n.526-527G>T
|
|
XR_242889.3:n.956-440G>T
|
|
|
XR_931290.1:n.1871G>T
|
|
|
NM_001129998.2:c.681-440G>T
|
NP_001123470.1:n.681-440G>T
|
|
NM_001319241.1:c.372-440G>T
|
NP_001306170.1:n.372-440G>T
|
|
NM_001319242.1:c.*2145G>T
|
NP_001306171.1:n.*2145G>T
|
|
NM_205852.3:c.*2145G>T
|
NP_995324.2:n.*2145G>T
|
|
NR_135049.1:n.961-440G>T
|
|
|
XM_011520658.2:c.654-440G>T
|
XP_011518960.1:n.654-440G>T
|
|
XM_011520663.2:c.526-440G>T
|
XP_011518965.1:n.526-440G>T
|
|
XM_017019295.1:c.372-440G>T
|
XP_016874784.1:n.372-440G>T
|
|
XM_024448976.1:c.681-527G>T
|
XP_024304744.1:n.681-527G>T
|
|
XM_024448977.1:c.*2152G>T
|
XP_024304745.1:n.*2152G>T
|
|
XR_002957401.1:n.106-1743C>A
|
|
|
NM_001129998.3:c.681-440G>T
MANE Select
|
NP_001123470.1:n.681-440G>T
|
|
NM_001387138.1:c.681-527G>T
|
NP_001374067.1:n.681-527G>T
|
|
NR_169587.1:n.258-1743C>A
|
|
|