ENST00000260197.12:c.4778G>T
MANE Select
|
ENSP00000260197.6:p.Arg1593Met
|
|
ENST00000260197.11:c.4778G>T
|
ENSP00000260197.6:p.Arg1593Met
|
|
ENST00000525532.5:c.1610G>T
|
ENSP00000434634.1:p.Arg537Met
|
|
ENST00000527934.1:c.623G>T
|
ENSP00000435405.1:p.Arg208Met
|
|
ENST00000532694.5:c.1316G>T
|
ENSP00000432131.1:p.Arg439Met
|
|
ENST00000534286.5:c.1508G>T
|
ENSP00000436447.1:p.Arg503Met
|
|
NM_003105.5:c.4778G>T
|
NP_003096.1:p.Arg1593Met
|
|
XM_011542963.1:c.4664G>T
|
XP_011541265.1:p.Arg1555Met
|
|
XM_011542964.1:c.4778G>T
|
XP_011541266.1:p.Arg1593Met
|
|
XM_011542965.1:c.3239G>T
|
XP_011541267.1:p.Arg1080Met
|
|
XM_011542966.1:c.2138G>T
|
XP_011541268.1:p.Arg713Met
|
|
XM_011542967.1:c.1610G>T
|
XP_011541269.1:p.Arg537Met
|
|
XM_011542963.3:c.4664G>T
|
XP_011541265.1:p.Arg1555Met
|
|
XM_011542965.3:c.3239G>T
|
XP_011541267.1:p.Arg1080Met
|
|
XM_011542967.3:c.1610G>T
|
XP_011541269.1:p.Arg537Met
|
|
XM_017018169.2:c.4466G>T
|
XP_016873658.1:p.Arg1489Met
|
|
XM_017018170.2:c.4253G>T
|
XP_016873659.1:p.Arg1418Met
|
|
XM_017018171.1:c.4778G>T
|
XP_016873660.1:p.Arg1593Met
|
|
XM_017018172.2:c.2138G>T
|
XP_016873661.1:p.Arg713Met
|
|
NM_003105.6:c.4778G>T
MANE Select
|
NP_003096.2:p.Arg1593Met
|
|